Next Article in Journal
A Single Liver Metastasis from Pleural Biphasic Mesothelioma
Next Article in Special Issue
Effect of Mutated ids Overexpression on IDS Enzyme Activity and Developmental Phenotypes in Zebrafish Embryos: A Valuable Index for Assessing Critical Point-Mutations Associated with Mucopolysaccharidosis Type II Occurrence in Humans
Previous Article in Journal
Ultrasound Features of a Uterine Perivascular Epithelioid Cell Tumor (PEComa): Case Report and Literature Review
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:

Hearing Loss in Mucopolysaccharidoses: Current Knowledge and Future Directions

Jeremy Wolfberg
Keerthana Chintalapati
Shunji Tomatsu
1,4,5,6 and
Kyoko Nagao
Nemours Biomedical Research, Nemours/Alfred I. duPont Hospital for Children, Wilmington, DE 19803, USA
Department of Communication Sciences and Disorders, West Chester University, West Chester, PA 19383, USA
Department of Biology, Washington University in Saint Louis, Saint Louis, MO 63130, USA
Department of Pediatrics, Thomas Jefferson University, Philadelphia, PA 19107, USA
Department of Pediatrics, Graduate School of Medicine, Gifu University, Gifu 501-1194, Japan
Department of Pediatrics, Shimane University, Shimane 690-8504, Japan
College of Health Sciences, University of Delaware, Newark, DE 19716, USA
Author to whom correspondence should be addressed.
Diagnostics 2020, 10(8), 554;
Submission received: 2 July 2020 / Revised: 31 July 2020 / Accepted: 2 August 2020 / Published: 4 August 2020
(This article belongs to the Special Issue Mucopolysaccharidoses: Diagnosis, Treatment, and Management 2.0)


Mucopolysaccharidoses (MPS) are a group of lysosomal storage disorders caused by a deficiency of one of the enzymes involved in the degradation of glycosaminoglycans. Hearing loss is a common clinical presentation in MPS. This paper reviews the literature on hearing loss for each of the seven recognized subtypes of MPS. Hearing loss was found to be common in MPS I, II, III, IVA, VI, and VII, and absent from MPS IVB and MPS IX. MPS VI presents primarily with conductive hearing loss, while the other subtypes (MPS I, MPS II, MPS III, MPS IVA, and MPS VII) can present with any type of hearing loss (conductive, sensorineural, or mixed hearing loss). The sensorineural component develops as the disease progresses, but there is no consensus on the etiology of the sensorineural component. Enzyme replacement therapy (ERT) is the most common therapy utilized for MPS, but the effects of ERT on hearing function have been inconclusive. This review highlights a need for more comprehensive and multidisciplinary research on hearing function that includes behavioral testing, objective testing, and temporal bone imaging. This information would allow for better understanding of the progression and etiology of hearing loss. Owing to the prevalence of hearing loss in MPS, early diagnosis of hearing loss and annual comprehensive audiological evaluations are recommended.

1. Introduction

Mucopolysaccharidoses (MPS) represent a group of rare lysosomal storage disorders. There are currently seven recognized subtypes of MPS caused by a deficiency of one of eleven enzymes involved in the degradation of glycosaminoglycans (GAGs), as shown in Table 1.
Most of the subtypes are caused by autosomal recessive inheritance, with only MPS type II being caused by X-linked recessive inheritance [8]. Both conductive and sensorineural hearing loss are common across the MPS subtypes. However, the literature focusing on hearing health in MPS is scarce, and many of the past studies are based on small samples. Large sample studies investigating enzyme replacement therapy (ERT) in MPS often report ERT effects on hearing, but detailed information is not available in general. Recently, there has been an increasing number of research papers focused on detailed hearing function. Below, we will review the literature on hearing loss in each MPS subtype. Table 2 shows a summary of references focused on audiological findings in patients with MPS.

2. Mucopolysaccharidosis Type I (Hurler Syndrome)

MPS type I (MPS I) is caused by a deficiency in the lysosomal enzyme alpha-L-iduronidase, which is involved in the degradation of dermatan sulfate (DS) and heparan sulfate (HS) [1]. MPS I was previously divided into three categories based on phenotype severity; that is, Hurler syndrome (OMIM 607014; the severe phenotype), Hurler–Scheie syndrome (OMIM 607015; the intermediate phenotype), and Scheie syndrome (OMIM 607016; the mild phenotype) [47]. Owing to overlapping symptoms in the three categories, MPS I is now categorized as severe, which includes Hurler syndrome, or attenuated, which includes Hurler–Scheie syndrome and Scheie syndrome [47,48,49]. The severe phenotype is most common, with a reported rate of 60.9% [47]. Neurological impairment is present in the severe phenotype, but is often absent from the attenuated phenotype [48]. Symptoms common in both phenotypes include coarse facial features, corneal clouding, hepatomegaly, cardiac valve abnormalities, hernia, lumbar kyphosis (gibbus), hearing loss, upper airway infection, and sleep apnea [47,48,49].

2.1. Types and Cause of Hearing Loss

Hearing loss is common in both the severe and attenuated phenotypes [49]. Reported rates of hearing loss range from 76.2% to 100% [10,20,21,22]. Hearing loss can present as conductive, sensorineural, or mixed [20]. Severity ranges from mild to severe, with mild and moderately severe being most common [10]. Chronic otitis media is also common, with an estimated rate of 89.1% [22]. The conductive component is attributed to frequent otitis media, a thickened tympanic membrane, and ossicular chain abnormalities [21,23,24,48]. The sensorineural component is believed to develop later in life after conductive hearing loss is already present [50]. Later development of sensorineural hearing loss was described in a MPS I murine model [26]. Inner ear abnormalities have been described in histopathological examination of patients with MPS I, but there is currently no consensus regarding the etiology of sensorineural hearing loss. Inner ear abnormalities that have been described include degeneration of the organ of Corti [23,24,27], damage to the stria vascularis [27], a significant decrease of both outer and inner cochlear hair cells [24], and damage to Reissner’s membrane [23,27]. A deposit of GAGs was also found on the vestibulo-cochlear nerve [23]. While cochlear and retrocochlear damage have been described, further research is needed to determine the precise etiology of the sensorineural component.

2.2. Efficacy of Clinical Treatments on Hearing

Hematopoietic stem cell transplantation (HSCT) and ERT are common treatments for MPS I. HSCT is primarily utilized to treat the severe phenotype, while ERT with laronidase is commonly utilized with the attenuated phenotype [47]. Several studies have described hearing improvement after HSCT [18,25]. It is recommended that HSCT occurs early in life, as improvement of sensorineural hearing loss was most significant in patients who received HSCT at 25 months or younger [18]. HSCT can be a dangerous treatment and has an estimated mortality rate of 11% [25]. ERT has been described as an effective method for changing the natural history of the MPS I attenuated form [51,52]. Studies have described that ERT does not improve audiological findings in patients with MPS I [21,53]. In a report of two case studies, a patient with conductive hearing loss experienced improved audiological findings after ERT, while a patient with mixed hearing loss did not exhibit audiological improvement [54]. Further research is needed to determine the effects of ERT on the conductive and sensorineural components of hearing loss. Particularly, the effects of ERT on inner ear function and the auditory neurophysiological responses at both brainstem and cortical levels would reveal detailed effects on sensorineural hearing function. Tympanostomy tubes are also commonly placed in patients with MPS I, with a reported rate of 78.2% [22]. Multiple tympanostomy tube placements are often required [19].

3. Mucopolysaccharidosis Type II (Hunter Syndrome)

MPS type II (MPS II), also known as Hunter syndrome (OMIM 309900), is the only subtype of MPS that is caused by X-linked recessive inheritance. Males are predominantly affected, but rare female cases have been reported [28,55]. Hunter syndrome is caused by a deficiency in the lysosomal enzyme iduronate-2-sulfatase [2], which is involved in the degradation of DS and HS [1]. MPS II is often divided into two categories (i.e., an attenuated or mild phenotype and a severe phenotype), but there is a wide spectrum of symptoms and phenotype severities [56]. The severe phenotype is characterized by early neurological impairment and intellectual disability, while the attenuated or mild phenotype only presents with mild neurological impairment [1,30]. Heart disease, skeletal deformities, upper respiratory tract infections, abdominal distention, developmental delays, and hearing loss are common in both phenotypes of MPS II [1,28,29,30,56].

3.1. Audiological Findings

Audiological findings have been well documented in MPS II. An MPS II international registry reported hearing loss data from 554 patients [28]. In a recent study of audiological findings of various types of MPS, 73.4% (91/124) of patients were diagnosed with MPS II [12]. Hearing loss is common, with reported rates ranging from 67.3% to 94%. Otitis media is also common, with a reported rate of 72.4% [28]. Hearing loss in MPS II has been described as progressive [12,15], with an estimated rate of loss at 1 dBHL per year [28]. Sensorineural hearing loss and mixed hearing loss are the most common types of hearing loss. The severity of hearing loss varies, with patients ranging from mild to profound [12,14,28]. Lack of cooperation has been cited as a barrier to determining the type and severity of hearing loss [12]. Owing to cognitive impairments, different modes of assessments, such as visual reinforcement audiometry, are often utilized to collect more accurate data [10]. Neurophysiological procedures such as otoacoustic emissions (OAEs) and auditory brainstem responses (ABRs) can be used in some cases to assess hearing function and provide timely clinical interventions to manage progressive hearing loss [57]. It is recommended that neurophysiological procedures be done without anesthesia, as MPS patients have a higher risk of complications from sedation [58,59,60].

3.2. Causes of Hearing Loss

Hunter syndrome presents with components of conductive and sensorineural hearing loss. Patients often first experience conductive hearing loss when they are younger. During childhood, sensorineural components emerge and lead to severe sensorineural hearing loss or mixed hearing loss. Owing to deposits of GAGs in the Eustachian tube and middle ear, frequent otitis media is common in patients with MPS II [9]. Accumulation of GAGs also leads to dysostosis of the ossicular chain and tympanic membrane scarring [61]. There is a lack of research on the sensorineural components in MPS II. Further research would be needed to determine if the sensorineural component is congenial or acquired owing to deposits of GAGs in the inner ear [9].

3.3. Efficacy of Clinical Treatments on Hearing

ERT has been described as a safe and effective treatment option for patients with MPS II [30]. ERT is most effective when started early in MPS II patients [61]. A murine study found that ERT was able to improve hearing levels and reduce the collection of GAGs in the outer and middle ear, but showed no effect on the inner ear [31]. Human research is needed on the efficacy of ERT for improving auditory function. Inserting tympanostomy tubes is an effective method for improving the conductive component of hearing loss by aerating the middle ear. Insertion of tympanostomy tubes has a reported rate of 49.6% [28]. Hearing aids are often utilized for patients with sensorineural hearing loss. Hearing aid use has a reported rate of 40.6% in patients with MPS II [28]. Recently, an adolescent patient with MPS II experienced hearing improvement after the implantation of a cochlear implant [62].

4. Mucopolysaccharidosis Type III (Sanfilippo Syndrome)

MPS type III (MPS III), also known as Sanfilippo syndrome, currently has four recognized subtypes (i.e., type A, B, C, and D), which are each caused by a deficiency to one of four enzymes that are responsible for the degradation of heparan sulfate, as shown in Table 3. Declined neurocognitive functions such as developmental delays, language delay, aggressive behaviors, and hearing loss are common among patients with all subtypes of MPS III [3,32,63,64,65], and their causes are often attributed to the degeneration of the central nervous system (CNS) [3]. Reported incidences and estimated prevalence vary by countries or regions of previous studies [66]. MPS IIIA and IIIB are common subtypes among the four, while MPS IIIC and IIID are rarer forms [66].

4.1. Audiological Findings

There is limited research focusing on the assessment of auditory function in human patients with MPS III. Only a handful of studies have reported clinical symptoms of patients with MPS IIIC and MPS IIID [3,67,68], and detailed descriptions of the progression of hearing loss are not well documented in these subtypes. Because MPS III affects the CNS, standard hearing assessment that requires patients’ compliance is challenging in many cases. Poor documentation of auditory function in MPS III may be owing to an inability to accurately collect data, as collecting audiometric data has been described as being difficult in patients with MPS III because of behavioral problems [3,67,68]. Previously reported rates of hearing loss are 87% (48/55) in MPS IIIA [32], 100% (3/3) in MPS IIIB [69], 75% (15/20) in MPS IIIC [67], and 25% (1/4) in MPS IIID [64]. The severity of hearing loss ranged from mild to moderate-severe in MPS IIIA [32] and moderate to severe in MPS IIIB [69]. Sensorineural hearing loss was the most common type of hearing loss [10,12,32,69], but the type of hearing loss was not determined in some patients because comprehensive hearing assessment was difficult to conduct or not available [65]. Conductive issues also appear early in life, as otitis media has a reported rate of 91%, and tympanostomy tubes are placed in most patients before 5 years [32]. While both conductive and sensorineural components have been shown to be present in patients with Sanfilippo syndrome, more research focused on audiometric findings and auditory function in human patients would be valuable in determining the need for hearing services to improve quality of life. Cortical potentials can be used to assess auditory processing abnormality in patients with impaired cognitive function.

4.2. Cause of Hearing Loss

A murine model of MPS IIIB displayed abnormalities in the middle ear, otitis media, hair cell loss in the inner ear, and damage to outer sulcus and pillar cells in the organ of Corti, affecting the base of the cochlea [31]. Chronic otitis media in MPS III contribute to the conductive hearing loss. It is likely that the disease simultaneously affects both the inner ear and the CNS, but further research is needed to understand the progression of hearing loss in MPS III.

4.3. Efficacy of Clinical Treatments on Hearing

Currently, there are no treatments available for MPS III. Severe impairment of the CNS has been described as a barrier for treatment development [70]. Bone marrow transplantation (BMT) and umbilical cord stem cell transplantation do not ameliorate the impairments to the CNS in MPS III [71,72,73]. ERT is also ineffective, as enzymes are not able to cross the blood–brain barrier [70]. The use of Genistein, an isoflavone, in substrate reduction therapy has been described as a safe and potentially effective method to reduce the collection of GAGs, but further research is needed to determine the therapeutic efficacy of genistein at improving neurological and auditory function [74]. Murine models have found that intracranial adeno-associated virus (AAV) gene therapy improved auditory function, as assessed by ABR, and reduced GAGs levels in the CNS, middle ear, and inner ear [75,76]. Similar results were also found in murine models that utilized a combination of intracranial AAV gene therapy and BMT [76]. Human research is needed to determine the efficacy of gene therapy and the combined use of gene therapy and BMT on neurological and auditory function.

5. Mucopolysaccharidosis Type IV (Morquio Syndrome)

MPS type IV (MPS IV), also known as Morquio syndrome, is divided into two subtypes; that is, MPS IVA (OMIM 253000) and MPS IVB (OMIM 253010). MPS IVA is caused by a deficiency in the lysosomal enzyme N-acetylgalactosamine-6-sulfate sulfatase, which is involved in the degradation of chondroitin-6-sulfate and keratan sulfate (KS) [4]. MPS IVB is caused by a deficiency in the lysosomal enzyme beta-galactosidase, which is involved in the degradation of KS [5]. Ninety-five percent of MPS IV patients present with MPS IVA [77]. MPS IVA presents with a wide range of phenotypes, ranging from an attenuated form to a severe form. Bone deformities to the knees, back-spine, chest, wrist, hips, legs, and ankles are common [78]. Other common symptoms include short stature, upper and lower airway obstruction, hearing loss, cardiac abnormalities, corneal clouding, and dental abnormalities [78,79,80,81]. MPS IVB presents with a milder phenotype than MPS IVA [82,83].

5.1. Hearing Loss

Hearing loss is common in MPS IVA [11,14,34,35], but patients with MPS IVB have been described as having normal hearing [34,82,84]. Limited research was found on the audiological assessment of patients with MPS IVA, but previous studies suggest that patients with MPS IVA experience hearing loss as the disease progresses. Reported rates of hearing loss range from 67% [11,14] to 94% [35]. Hearing loss can present as conductive, sensorineural, or mixed with severity ranging from mild to profound. Recurrent otitis media are also common in patients with MPS IVA. Similar to other types of MPS, conductive hearing loss often presents in younger patients, while sensorineural or mixed hearing loss develops later. The study by Riedner and Levin found that conductive hearing loss was present in all patients younger than 8 years old, while sensorineural or mixed hearing loss was found in older patients [35]. The conductive component is likely caused by recurrent otitis media and a collection of GAGs on the tympanic membrane and ossicular chain [34]. The etiology of the sensorineural component remains unknown. Thanks to absent distortion products otoacoustic emissions (DPOAEs) and decreased ABR, Nagao et al. described hair cell loss as a likely contributing factor to sensorineural hearing loss [34]. Animal models have also described the role of KS in the inner ear [36], but further research is needed to determine the etiology in humans. Recently, a relationship has been described between height (skeletal severity) and hearing loss severity in patients with MPS IVA [34]. It is recommended that patients receive an annual audiological assessment that includes both behavior and electrophysiological testing [34,80].

5.2. Efficacy of Clinical Treatments on Hearing

ERT with elosulfase alfa, or Vimizim, is a safe and commonly utilized therapy for patients with MPS IVA [85,86,87]. While hearing improvement after ERT was described in a case report [88], further research with a larger sample size is needed to determine the efficacy of ERT on improving hearing. HSCT has been described in MPS IVA case studies, but the impact on hearing was not assessed in any of these studies [87,89,90]. AAV gene therapy [91,92] and substrate reduction therapy [93] have been studied in animal models, but the impact of hearing has not been assessed. Tympanostomy tubes are placed in some patients to help alleviate the conductive component, with a reported rate of 33% in MPS IVA [78]. Recently, an MPS IVA post-lingual patient with severe to profound sensorineural hearing loss presented with hearing improvement after the implantation of a cochlear implant [94].

6. Mucopolysaccharidosis Type VI (Maroteaux–Lamy Syndrome)

MPS type VI (MPS VI), also known as Maroteaux–Lamy syndrome (OMIM 253200), is a rare autosomal recessive lysosomal storage disorder caused by the deficiency of arylsulfatase B (ARSB) [6]. The reduced or absent activity of this enzyme leads to the accumulation of GAGs in the lysosomes and a consequential decline in the function of multiple organ systems. Symptoms usually appear in early childhood and include macrocephaly, heart problems, upper respiratory infections, umbilical hernias, hepatomegaly, corneal clouding, chronic otitis media, and hearing loss [95].

6.1. Hearing Loss in MPS VI

There are a few studies that have specifically examined hearing issues in MPS VI [10,11,14]. Most of the previous studies reported hearing or ear problems in relation to the effects of ERT. Recurrent acute otitis media are a common problem in patients with MPS VI [96]. Most patients with MPS VI suffer from mild to moderate conductive hearing loss [10,11,37,96]. A recent retrospective study of five patients with MPS VI reported that, while conductive hearing loss is common, it seems to be temporary and can be treated through surgical interventions such as tympanostomy tube placement [97]. Recurrent otitis media with effusion persisted into adolescents, and multiple sets of tympanostomy tubes were common among the patients with MPS VI. It has been reported that some patients exhibit sensorineural or mixed hearing loss [10,14], but it is rare that patients with MPS VI have sensorineural hearing loss [98]. Although studies have reported audiological findings in MPS VI, the progression of hearing loss as well as their onset are not well-documented.

6.2. Efficacy of Clinical Treatment on Hearing

The standard treatment for hearing issues in patients with MPS VI is tympanostomy tube placement to reduce recurrent otitis media [96]. However, tympanostomy tube placement may serve only as a temporary solution to middle ear issues, as the tubes lose function and fall out after a few years. Without the presence of any otolaryngologic interventions such as tympanostomy tube placement, hearing issues can progress and lead to severe or permanent hearing loss [97]. As for the ERT effects on hearing in patients with MPS VI, the results are still inconclusive [37,38,39,40,53]. Previous studies have indicated an unchanging hearing status after ERT in some patients, whereas other studies have indicated hearing improvement [38,39,40], even in the patient with sensorineural hearing loss. It is not clear how ERT improved sensorineural hearing loss in MPS VI. ERT could reduce upper respiratory infections and ear infections, and subsequentially reduce the occurrence of ear infections and prevent conductive hearing loss.

7. Mucopolysaccharidosis Type VII (Sly Syndrome)

MPS type VII (MPS VII), also known as Sly syndrome (OMIM 253220), is one of the rarer forms of MPS, with an estimated incidence of 1:300,000 to 1:2,000,000 live births [8,41]. Sly syndrome is caused by a deficiency in the lysosomal enzyme glucuronidase, which is involved in the degradation of chondroitin sulfate, DS, and HS [1]. Skeletal dysplasia, cognitive impairments, heart abnormalities, and hearing loss are common in patients with MPS VII [1,41,45,99].

7.1. Causes of Hearing Loss

Murine models of MPS VII have displayed abnormalities in the middle and inner ear. The conductive component has been attributed to cerumen impaction, recurrent otitis media, and ossicle articular alterations [45]. Inner ear pathology in a murine model suggested that the sensorineural component is attributed to the assembly of GAGs, severely affecting inner ear structures such as Reissner’s membrane, spiral limbus, spiral ligament, spiral prominence, and spiral ganglion [42]. Sensorineural deficits were observed at a later onset than conductive deficits.

7.2. Audiological Findings

Limited research was found focusing on the assessment of auditory function in human patients with MPS VII. This may be because of the low incidence and rare nature of Sly syndrome. Recent studies on the audiological assessment of various types of MPS have not included any participants with MPS VII [10,11,12,14]. In a physician’s medical history survey of 56 patients with Sly syndrome, sensorineural hearing loss was present in 41% of participants [41]. A case study presents audiometric results from a patient with a rare and milder phenotype, as the patient lived to the age of 52 years [100]. At the age of 13, this patient was described as having mixed bilateral hearing loss, with hearing thresholds determined to be 50 dB Hearing Level (dB HL) in the right ear and 40 dB HL in the left ear [100]. As this is a rare and milder phenotype, this may not be representative of typical thresholds and audiological diagnoses. Several murine models investigating the effects of various therapies have described audiological findings in mice with MPS VII. In a murine study investigating the effects of syngeneic BMT, the untreated murine model presented with an ABR that was 42 dB higher than the normal untreated mice [44]. A murine study investigating the effects of ERT states that a stimulus greater than 60 dB was needed at every frequency tested in order to elicit an ABR waveform response [43].

7.3. Efficacy of Clinical Treatment on Hearing

Murine models have been utilized to observe the efficacity of several therapy methods on the improvement of audiometric results and pathological findings [43,44,101]. Syngeneic BMT improved ABR to within normal limits at 11 weeks of age, reduced the severity of hearing loss at 33 weeks, and decreased the severity of otitis media and pathological abnormalities in a murine model [44,101,102]. ERT initiated at birth in mice led to the improvement in ABR thresholds, reduction in ossicular abnormalities, and a decrease in middle ear inflammation [43]. Treatment is described as being more effective when initiated at birth in both BMT and ERT [101]. Recently, the ERT vestronidase alfa, or Mepsevii, was approved for MPS VII in humans [103,104], but current research has not included audiological findings. Human research is needed to determine the efficacy of BMT and ERT in reducing hearing loss and audiological pathology.

8. Mucopolysaccharidosis Type IX (Natowicz Syndrome)

MPS type IX (MPS IX), also known as Natowicz syndrome, is an extremely rare autosomal recessive disorder that causes hyaluronidase deficiency (OMIM 601492). Currently, only four patients have been reported to have MPS IX and the corresponding hyaluronan accumulation [7]. The first report of MPS IX was in 1996, where a 14-year-old patient exhibited short stature and multiple tissue masses. Upon examination of this patient, a deficiency of hyaluronidase was identified [7,104,105]. The other three reported cases of MPS IX were within a single consanguineous family, where all patients exhibited knee or hip pain and joint swelling [46].

8.1. Hearing Issues

Unlike other MPS types, patients with MPS IX do not exhibit hearing loss among the few known reported cases [7,46]. Although it was reported that the first patient with MPS IX had frequent episodes of otitis media, the patient did not exhibit hearing loss or any speech and language issues [7]. No hearing issues were found in the other three cases of MPS IX [46].

8.2. Animal Models

Although there is only a small number of reported cases, animal models can give us insight on varied clinical symptoms and treatment options for patients with MPS IX. MPS IX is caused by the deficiency of hyaluronidase 1 (HYAL1) [105]. Murine models suggest that HYAL1 deficiency leads to joint pathology [106]. HYAL1-null mice had normal appearance, fertility, and tissue morphology. Osteoarthritis was found to be a primary indicator of HYAL1 deficiency [106,107]. Murine models have also shown increased expression of the hyaluronidase 3 (HYAL3) gene in the liver and the testes of HYAL1-null mice [106,107]. It is proposed that the HYAL3 gene may compensate HYAL1 deficiency in MPS IX [106]. Furthermore, animal models suggest that there may be a new subtype of MPS in humans that has not been identified [106,107,108]. Mice with hyaluronidase 2 (HYAL2) deficiency developed skeletal defects and cardiac anomalies [108].

9. Discussion

This article provides a review of the literature on audiological findings in patients with each of the recognized subtypes of MPS. According to the current literature, hearing loss is common in most of the subtypes of MPS; that is, MPS I (Hurler syndrome), MPS II (Hunter syndrome), MPS III (Sanfilippo syndrome), MPS IVA (Morquio syndrome type A), MPS VI (Maroteaux–Lamy syndrome), and MPS VII (Sly syndrome). Hearing loss is not present in patients with MPS IVB (Morquio syndrome type B) or MPS IX (Natowicz syndrome), although this is based on a small number of patients owing to the rarity of these subtypes. MPS VI is the only subtype that presents primarily with conductive hearing loss. The other subtypes (MPS I, MPS II, MPS III, MPS IVA, and MPS VII) can present with any type of hearing loss (conductive, sensorineural, or mixed hearing loss). In these subtypes, patients often first present with conductive hearing loss and later develop a sensorineural component, leading to sensorineural or mixed hearing loss. It is unclear why MPS VI is the only subtype that does not affect a sensorineural component in general. Sensorineural hearing loss has been reported in some rare cases with MPS VI, although it is not clear whether sensorineural hearing loss is owing to relatively slow progression of MPS VI. While CNS impairment is absent from patients with MPS VI, it is also absent from patients with MPS IVA [109], a subtype that presents with sensorineural and mixed hearing loss. Further research is needed to determine if there are pathophysiological differences between MPS VI and the other subtypes.
More comprehensive audiological and pathophysiological research is needed to develop a more precise understanding of the progression of hearing loss in each MPS subtype. In particular, understanding both onsets and etiology of sensorineural hearing loss is critical to provide appropriate clinical intervention to patients. Figure 1 illustrates pathophysiology of hearing loss in MPS. This figure provides a broad overview of the pathophysiology, as the progression of hearing loss differs depending on the MPS subtype. Deposits of GAGs in mucosal linings, connective tissue, cartilages, bones, and the CNS lead to many of the components contributing to hearing loss. Chronic otitis media or persistent middle ear effusion is common in all subtypes beyond early childhood and contributes to the conductive component of hearing loss. Susceptibility to viral infections in patients with MPS is likely the main cause of frequent middle ear effusion, which could lead to structural changes in the tympanic membrane and ossicular deformities. A vicious cycle present between airway narrowing, chronic otitis media, and collections of thick secretions is believed to further the progression of the conductive component. Tympanostomy tubes are effective at treating middle ear dysfunction, but multiple tube replacements are common in MPS. This can lead to tympanic membrane thickening and scaring. Tympanic membrane thickening and ossicular chain abnormalities have been described as a contributing factor to conductive hearing loss in MPS I [21,23], MPS II [61], MPS IVA [34], and MPS VII in a murine model [45]. There is currently no consensus on the etiology of the sensorineural component for any of the recognized subtypes. A reduction in outer and inner cochlear hair cells likely contributes to the sensorineural component, as this has been described in MPS I [24], MPS IV [34], and MPS IIIB in a murine model [44]. The accumulation of GAGs is believed to cause damage to structures in the inner ear. Abnormalities to the organ of Corti, Reissner’s membrane, stria vascularis, and vestibulo-cochlear nerve have been described [20,21,23,24,30,41], but there is no consensus on their prevalence, severity, or effect on sensorineural hearing loss. Hearing loss does not seem to appear only at certain frequency ranges among patients with MPS, yet more detailed analysis of hearing loss would be crucial to understand the progression of sensorineural hearing loss. While a collection of GAGs has been shown to cause cochlear and retrocochlear damage, more research is needed to determine a more precise onset and etiology of sensorineural hearing loss. It is suspected that disease severity and sensorineural hearing loss are correlated with each other, but the relationship between hearing test results and other clinical measures such as GAG levels or bone density measures has not been studied. Owing to the complex nature of hearing loss in MPS, multidisciplinary research studies including experts in audiology, otolaryngology, biochemistry, neurology, radiology, and genetics are recommended.
Treatment options vary depending on the MPS subtype. ERT is the most common treatment for MPS, with approved therapies available for [51,52], MPS II [30], MPS IVA [85,86,87], MPS VI [37], and MPS VII [103,104]. Research on the effects of ERT on audiological function has been inconclusive [53]. While case reports on MPS IVA [88] and MPS VI [38,39] have described hearing improvement after ERT, studies on MPS I [21] and MPS VI [37] have described no change in audiological function after ERT. A MPS II murine model found that ERT was able to improve the conductive component, but was unable to ameliorate the sensorineural component [31]. This was also exhibited in two patients with MPS I, where the patient with conductive hearing loss presented with improved hearing after ERT and the patient with mixed hearing loss did not experience any audiological improvement [54]. More comprehensive audiological research is needed to delineate the effects of ERT on the conductive and sensorineural components for each MPS subtype. HSCT has resulted in improved audiological function in MPS I [18,25], but the impact of hearing has not been studied in MPS IVA [87,89,90]. Owing to the high prevalence of hearing loss in most MPS subtypes, future studies on treatment efficacy should include comprehensive audiological evaluation.
This review highlights the need for more comprehensive audiological research for all subtypes of MPS. Previous studies on hearing loss have primarily utilized behavioral audiological testing and tympanometry. In addition to commonly reported pure tone average threshold levels, future research should report frequency specific hearing thresholds. Frequency specific information (e.g., averages of multiple audiograms from a given MPS subtype) would provide valuable insights into specific cochlear regions affected by MPS. OAE and ABR have occasionally been utilized, but these studies often do not provide detailed results. Temporal bone imaging is rarely utilized in the current literature. In addition to common behavioral audiological assessment, future research should utilize auditory neurophysiological assessment and temporal bone imaging as a part of a comprehensive assessment. A recent paper by van den Broek et al. is a prime example of a comprehensive assessment of auditory function [19]. This retrospective review on the effects of hematopoietic cell transplantation on hearing loss utilized pure tone audiometry, neurophysiological assessment (ABR), and imaging. Owing to respiratory, skeletal, pulmonary, and cardiovascular abnormalities, MPS patients have an increased risk of sedation complications [58,59,60]. Because patients with MPS undergo radiological and neuroradiological imaging procedure for their skeletal issues, it is desirable to obtain temporal bone imaging to assess the ear structures without increasing risk of anesthesia. OAE and ABR can be conducted without general anesthesia. Comprehensive audiological research would provide a better understanding of the progression and etiology of hearing loss in each subtype of MPS. Identifying the etiology of the sensorineural hearing loss common in many patients with MPS would help clinicians to determine optimal clinical interventions precisely prescribed to each patient. A better understanding of the progression of hearing loss could also be used in the assessment of clinical intervention efficacy.
Finally, this review highlights the importance of early diagnosis of hearing loss and annual comprehensive audiological evaluation for patients with MPS. This is consistent with other recommendations found in the literature [10,11,12,13,14,15,16,17,19,34,80,110,111,112]. Owing to the high prevalence and progressive nature of hearing loss in MPS, regular audiological assessments are needed to determine the progression of hearing loss and the need for hearing aids or tympanostomy tube placement. Early detection and intervention can help in the improvement of quality of life for patients with MPS.

Author Contributions

Conceptualization, S.T. and K.N.; resources, J.W., K.C., and K.N.; data curation, J.W., K.C., and K.N.; writing—original draft preparation, J.W., K.C., S.T., and K.N.; writing—review and editing, J.W., K.C., S.T., and K.N.; visualization, J.W., K.C., S.T., and K.N.; supervision, K.N.; funding acquisition, S.T. and K.N. All authors have read and agreed to the published version of the manuscript.


This project and K.C. were supported by the Delaware INBRE program, with a grant from the National Institute of General Medical Sciences—NIGMS (P20 GM103446) from the National Institutes of Health and the State of Delaware. This publication was made possible by the Delaware INBRE program, supported by a grant from the National Institute of General Medical Sciences—NIGMS (P20 GM103446) from the National Institutes of Health and the State of Delaware.

Conflicts of Interest

The authors declare no conflict of interest.


ERTEnzyme replacement therapy
dB HLdB hearing level
DSDermatan sulfate
HSHeparan sulfate
HSCTHematopoietic stem cell transplantation
OAEOtoacoustic emissions
ABRAuditory brainstem response
CNSCentral nervous system
BMTBone marrow transplantation
AAVAdeno-associated virus
KSKeratan sulfate
DPOAEDistortion products otoacoustic emissions
ARSBArylsulfatase B
HYAL1Hyaluronidase 1
HYAL3Hyaluronidase 3
HYAL2Hyaluronidase 2
HLHearing loss


  1. Wraith, J.E.; Rogers, J.G.; Danks, D.M. The mucopolysaccharidoses. J. Paediatr. Child. Health 1987, 23, 329–334. [Google Scholar] [CrossRef] [PubMed]
  2. Demydchuk, M.; Hill, C.H.; Zhou, A.; Bunkóczi, G.; Stein, P.E.; Marchesan, D.; Deane, J.E.; Read, R.J. Insights into Hunter syndrome from the structure of iduronate-2-sulfatase. Nat. Commun. 2017, 8, 15786. [Google Scholar] [CrossRef] [PubMed]
  3. Andrade, F.; Aldámiz-Echevarría, L.; Llarena, M.; Couce, M.L. Sanfilippo syndrome: Overall review. Pediatr. Int. 2015, 57, 331–338. [Google Scholar] [CrossRef] [PubMed]
  4. Peracha, H.; Sawamoto, K.; Averill, L.; Kecskemethy, H.; Theroux, M.; Thacker, M.; Nagao, K.; Pizarro, C.; Mackenzie, W.; Kobayashi, H.; et al. Molecular genetics and metabolism, special edition: Diagnosis, Diagnosis and prognosis of Mucopolysaccharidosis IVA. Mol. Genet. Metab. 2018. [Google Scholar] [CrossRef] [PubMed]
  5. Shimada, T.; Tomatsu, S.; Mason, R.W.; Yasuda, E.; Mackenzie, W.G.; Hossain, J.; Shibata, Y.; Montaño, A.M.; Kubaski, F.; Giugliani, R.; et al. Di-sulfated Keratan Sulfate as a Novel Biomarker for Mucopolysaccharidosis II, IVA, and IVB. JIMD Rep. 2015, 21, 1–13. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Tomanin, R.; Karageorgos, L.; Zanetti, A.; Al-Sayed, M.; Bailey, M.; Miller, N.; Sakuraba, H.; Hopwood, J.J. Mucopolysaccharidosis type VI (MPS VI) and molecular analysis: Review and classification of published variants in the ARSB gene. Hum. Mutat. 2018, 39, 1788–1802. [Google Scholar] [CrossRef] [Green Version]
  7. Natowicz, M.R.; Short, M.P.; Wang, Y.; Dickersin, G.R.; Gebhardt, M.C.; Rosenthal, D.I.; Sims, K.B.; Rosenberg, A.E. Clinical and biochemical manifestations of hyaluronidase deficiency. N. Engl. J. Med. 1996, 335, 1029–1033. [Google Scholar] [CrossRef]
  8. Muenzer, J. Overview of the mucopolysaccharidoses. Rheumatology 2011, 50, v4–v12. [Google Scholar] [CrossRef] [Green Version]
  9. Simmons, M.A.; Bruce, I.A.; Penney, S.; Wraith, E.; Rothera, M.P. Otorhinolaryngological manifestations of the mucopolysaccharidoses. Int. J. Pediatr. Otorhinolaryngol. 2005, 69, 589–595. [Google Scholar] [CrossRef]
  10. Silveira, M.R.; Buriti, A.K.L.; Martins, A.M.; Gil, D.; Azevedo, M.F. Audiometric evaluation in individuals with mucopolysaccharidosis. Clin. Sao Paulo 2018, 73, e523. [Google Scholar] [CrossRef]
  11. Lenka, M.; Michal, J.; Pavel, J.; Vera, M.; Marketa, B.; Jiri, Z.; Martin, M. Otorhinolaryngological manifestations in 61 patients with mucopolysaccharidosis. Int. J. Pediatr. Otorhinolaryngol. 2020, 135, 110137. [Google Scholar] [CrossRef]
  12. Ahn, J.; Lee, J.J.; Park, S.-I.; Cho, S.-Y.; Jin, D.-K.; Cho, Y.-S.; Chung, W.-H.; Hong, S.-H.; Moon, I.J. Auditory Characteristics in Patients With Mucopolysaccharidosis. Otol. Neurotol. Off. Publ. Am. Otol. Soc. Am. Neurotol. Soc. Eur. Acad. Otol. Neurotol. 2019, 40, e955–e961. [Google Scholar] [CrossRef] [PubMed]
  13. Mesolella, M.; Cimmino, M.; Cantone, E.; Marino, A.; Cozzolino, M.; Della Casa, R.; Parenti, G.; Iengo, M. Management of otolaryngological manifestations in mucopolysaccharidoses: Our experience. Acta Otorhinolaryngol. Ital. Organo Uff. Della Soc. Ital. Otorinolaringol. E Chir. Cerv.-Facc. 2013, 33, 267–272. [Google Scholar]
  14. Lin, H.Y.; Shih, S.C.; Chuang, C.K.; Lee, K.S.; Chen, M.R.; Lin, H.C.; Chiu, P.C.; Niu, D.M.; Lin, S.P. Assessment of hearing loss by pure-tone audiometry in patients with mucopolysaccharidoses. Mol. Genet. Metab. 2014, 111, 533–538. [Google Scholar] [CrossRef]
  15. Vargas-Gamarra, M.F.; de Paula-Vernetta, C.; Vitoria Minana, I.; Ibanez-Alcaniz, I.; Cavalle-Garrido, L.; Alamar-Velazquez, A. Audiological findings in children with mucopolysaccharidoses type i-iv. Acta Otorrinolaringol. Esp. 2017, 68, 262–268. [Google Scholar] [CrossRef]
  16. Gokdogan, C.; Altinyay, S.; Gokdogan, O.; Tutar, H.; Gunduz, B.; Okur, I.; Tumer, L.; Kemaloglu, Y.K. Audiologic evaluations of children with mucopolysaccharidosis. Braz. J. Otorhinolaryngol. 2016, 82, 281–284. [Google Scholar] [CrossRef] [Green Version]
  17. Giraldo, L.J.M.; Arturo-Terranova, D.; Soto, J.M.S. Otorhinolaryngological Findings in Patients from Southwestern Colombia with Clinical, Enzymatic and Molecular Diagnosis of Mucopolysaccharidosis II, IV-A and VI. J. Inborn Errors Metab. Screen. 2020, 8, e20190006. [Google Scholar] [CrossRef]
  18. Da Costa, V.; O’Grady, G.; Jackson, L.; Kaylie, D.; Raynor, E. Improvements in Sensorineural Hearing Loss After Cord Blood Transplant in Patients With Mucopolysaccharidosis. Arch. Otolaryngol. Neck Surg. 2012, 138, 1071–1076. [Google Scholar] [CrossRef] [Green Version]
  19. van den Broek, B.T.A.; Smit, A.L.; Boelens, J.J.; van Hasselt, P.M. Hearing loss in patients with mucopolysaccharidoses-1 and -6 after hematopoietic cell transplantation: A longitudinal analysis. J. Inherit. Metab. Dis. 2020. [Google Scholar] [CrossRef]
  20. Aldenhoven, M.; Wynn, R.F.; Orchard, P.J.; O’Meara, A.; Veys, P.; Fischer, A.; Valayannopoulos, V.; Neven, B.; Rovelli, A.; Prasad, V.K.; et al. Long-term outcome of Hurler syndrome patients after hematopoietic cell transplantation: An international multicenter study. Blood 2015, 125, 2164–2172. [Google Scholar] [CrossRef] [Green Version]
  21. Dualibi, A.P.; Martins, A.M.; Moreira, G.A.; de Azevedo, M.F.; Fujita, R.R.; Pignatari, S.S.N. The impact of laronidase treatment in otolaryngological manifestations of patients with mucopolysaccharidosis. Braz. J. Otorhinolaryngol. 2016, 82, 522–528. [Google Scholar] [CrossRef] [Green Version]
  22. Kiely, B.T.; Kohler, J.L.; Coletti, H.Y.; Poe, M.D.; Escolar, M.L. Early disease progression of Hurler syndrome. Orphanet J. Rare Dis. 2017, 12, 32. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Friedmann, I.; Spellacy, E.; Crow, J.; Watts, R.W.E. Histopathological studies of the temporal bones in Hurler’s disease [mucopolysaccharidosis (MPS) IH]. J. Laryngol. Otol. 1985, 99, 29–41. [Google Scholar] [CrossRef]
  24. Kariya, S.; Schachern, P.A.; Nishizaki, K.; Paparella, M.M.; Cureoglu, S. Inner ear changes in mucopolysaccharidosis type I/Hurler syndrome. Otol. Neurotol. 2012, 33, 1323–1327. [Google Scholar] [CrossRef] [PubMed]
  25. Souillet, G.; Guffon, N.; Maire, I.; Pujol, M.; Taylor, P.; Sevin, F.; Bleyzac, N.; Mulier, C.; Durin, A.; Kebaili, K.; et al. Outcome of 27 patients with Hurler’s syndrome transplanted from either related or unrelated haematopoietic stem cell sources. Bone Marrow Transplant. 2003, 31, 1105–1117. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Schachern, P.A.; Cureoglu, S.; Tsuprun, V.; Paparella, M.M.; Whitley, C.B. Age-related functional and histopathological changes of the ear in the MPS I mouse. Int. J. Pediatr. Otorhinolaryngol. 2007, 71, 197–203. [Google Scholar] [CrossRef] [Green Version]
  27. Schachern, P.A.; Shea, D.A.; Paparella, M.M. Mucopolysaccharidosis I-H (Hurler’s syndrome) and human temporal bone histopathology. Ann. Otol. Rhinol. Laryngol. 1984, 93, 65–69. [Google Scholar] [CrossRef]
  28. Keilmann, A.; Nakarat, T.; Bruce, I.A.; Molter, D.; Malm, G.; HOS Investigators. Hearing loss in patients with mucopolysaccharidosis II: Data from HOS-the Hunter Outcome Survey. J. Inherit. Metab. Dis. 2012, 35, 343–353. [Google Scholar] [CrossRef]
  29. Chiong, M.A.D.; Canson, D.M.; Abacan, M.A.R.; Baluyot, M.M.P.; Cordero, C.P.; Silao, C.L.T. Clinical, biochemical and molecular characteristics of Filipino patients with mucopolysaccharidosis type II-Hunter syndrome. Orphanet J. Rare Dis. 2017, 12, 7. [Google Scholar] [CrossRef] [Green Version]
  30. Muenzer, J.; Wraith, J.E.; Beck, M.; Giugliani, R.; Harmatz, P.; Eng, C.M.; Vellodi, A.; Martin, R.; Ramaswami, U.; Gucsavas-Calikoglu, M.; et al. A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome). Genet. Med. 2006, 8, 465–473. [Google Scholar] [CrossRef] [Green Version]
  31. Hong, S.H.; Chu, H.; Kim, K.R.; Ko, M.H.; Kwon, S.Y.; Moon, I.J.; Chung, W.H.; Cho, Y.S.; Kim, C.H.; Suh, M.W.; et al. Auditory characteristics and therapeutic effects of enzyme replacement in mouse model of the mucopolysaccharidosis (MPS) II. Am. J. Med. Genet. Part A 2012, 158, 2131–2138. [Google Scholar] [CrossRef] [PubMed]
  32. Buhrman, D.; Thakkar, K.; Poe, M.; Escolar, M.L. Natural history of Sanfilippo syndrome type A. J. Inherit. Metab. Dis. 2014, 37, 431–437. [Google Scholar] [CrossRef] [PubMed]
  33. Heldermon, C.D.; Hennig, A.K.; Ohlemiller, K.K.; Ogilvie, J.M.; Herzog, E.D.; Breidenbach, A.; Vogler, C.; Wozniak, D.F.; Sands, M.S. Development of sensory, motor and behavioral deficits in the murine model of Sanfilippo syndrome type B. PLoS ONE 2007, 2, e772. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Nagao, K.; Morlet, T.; Haley, E.; Padilla, J.; Nemith, J.; Mason, R.W.; Tomatsu, S. Neurophysiology of hearing in patients with mucopolysaccharidosis type IV. Mol. Genet. Metab. 2018, 123, 472–478. [Google Scholar] [CrossRef] [PubMed]
  35. Riedner, E.D.; Levin, L.S. Hearing patterns in Morquio’s syndrome (mucopolysaccharidosis IV). Arch. Otolaryngol. 1977, 103, 518–520. [Google Scholar] [CrossRef] [PubMed]
  36. Swartz, D.J.; Santi, P.A. Immunohistochemical localization of keratan sulfate in the chinchilla inner ear. Hear. Res. 1997, 109, 92–101. [Google Scholar] [CrossRef]
  37. Gomes, D.F.; Gallo, L.G.; Leite, B.F.; Silva, R.B.; da Silva, E.N. Clinical effectiveness of enzyme replacement therapy with galsulfase in mucopolysaccharidosis type VI treatment: Systematic review. J. Inherit. Metab. Dis. 2019, 42, 66–76. [Google Scholar] [CrossRef]
  38. Furujo, M.; Kosuga, M.; Okuyama, T. Enzyme replacement therapy attenuates disease progression in two Japanese siblings with mucopolysaccharidosis type VI: 10-Year follow up. Mol. Genet. Metab. Rep. 2017, 13, 69–75. [Google Scholar] [CrossRef]
  39. Harmatz, P.; Garcia, P.; Guffon, N.; Randolph, L.M.; Shediac, R.; Braunlin, E.; Lachman, R.S.; Decker, C. Galsulfase (Naglazyme(R)) therapy in infants with mucopolysaccharidosis VI. J. Inherit. Metab. Dis. 2014, 37, 277–287. [Google Scholar] [CrossRef] [Green Version]
  40. Horovitz, D.D.G.; Magalhães, T.S.P.C.; Acosta, A.; Ribeiro, E.M.; Giuliani, L.R.; Palhares, D.B.; Kim, C.A.; de Paula, A.C.; Kerstenestzy, M.; Pianovski, M.A.D.; et al. Enzyme replacement therapy with galsulfase in 34 children younger than five years of age with MPS VI. Mol. Genet. Metab. 2013, 109, 62–69. [Google Scholar] [CrossRef] [Green Version]
  41. Montaño, A.M.; Lock-Hock, N.; Steiner, R.D.; Graham, B.H.; Szlago, M.; Greenstein, R.; Pineda, M.; Gonzalez-Meneses, A.; Çoker, M.; Bartholomew, D.; et al. Clinical course of sly syndrome (mucopolysaccharidosis type VII). J. Med. Genet. 2016, 53, 403–418. [Google Scholar] [CrossRef] [PubMed]
  42. Ohlemiller, K.K.; Hennig, A.K.; Lett, J.M.; Heidbreder, A.F.; Sands, M.S. Inner ear pathology in the mucopolysaccharidosis VII mouse. Hear. Res. 2002, 169, 69–84. [Google Scholar] [CrossRef]
  43. O’Connor, L.H.; Erway, L.C.; Vogler, C.A.; Sly, W.S.; Nicholes, A.; Grubb, J.; Holmberg, S.W.; Levy, B.; Sands, M.S. Enzyme replacement therapy for murine mucopolysaccharidosis type VII leads to improvements in behavior and auditory function. J. Clin. Investig. 1998, 101, 1394–1400. [Google Scholar] [CrossRef] [PubMed]
  44. Sands, M.S.; Erway, L.C.; Vogler, C.; Sly, W.S.; Birkenmeier, E.H. Syngeneic bone marrow transplantation reduces the hearing loss associated with murine mucopolysaccharidosis type VII. Blood 1995, 86, 2033–2040. [Google Scholar] [CrossRef]
  45. Berry, C.L.; Vogler, C.; Galvin, N.J.; Birkenmeier, E.H.; Sly, W.S. Pathology of the ear in murine mucopolysaccharidosis type VII. Morphologic correlates of hearing loss. Lab. Investig. J. Tech. Methods Pathol. 1994, 71, 438–445. [Google Scholar]
  46. Imundo, L.; Leduc, C.A.; Guha, S.; Brown, M.; Perino, G.; Gushulak, L.; Triggs-Raine, B.; Chung, W.K. A complete deficiency of Hyaluronoglucosaminidase 1 (HYAL1) presenting as familial juvenile idiopathic arthritis. J. Inherit. Metab. Dis. 2011, 34, 1013–1022. [Google Scholar] [CrossRef]
  47. Beck, M.; Arn, P.; Giugliani, R.; Muenzer, J.; Okuyama, T.; Taylor, J.; Fallet, S. The natural history of MPS I: Global perspectives from the MPS I Registry. Genet. Med. 2014, 16, 759–765. [Google Scholar] [CrossRef] [Green Version]
  48. Kubaski, F.; de Oliveira Poswar, F.; Michelin-Tirelli, K.; Matte, U.; Horovitz, D.D.; Barth, A.L.; Baldo, G.; Vairo, F.; Giugliani, R. Mucopolysaccharidosis Type I. Diagn. Basel Switz. 2020, 10, 161. [Google Scholar] [CrossRef] [Green Version]
  49. Muenzer, J.; Wraith, J.E.; Clarke, L.A. Mucopolysaccharidosis I: Management and treatment guidelines. Pediatrics 2009, 123, 19–29. [Google Scholar] [CrossRef]
  50. Giugliani, R.; Harmatz, P.; Lin, S.-P.; Scarpa, M. Assessing the impact of the five senses on quality of life in mucopolysaccharidoses. Orphanet J. Rare Dis. 2020, 15, 97. [Google Scholar] [CrossRef]
  51. Eisengart, J.B.; Jarnes, J.; Ahmed, A.; Nestrasil, I.; Ziegler, R.; Delaney, K.; Shapiro, E.; Whitley, C. Long-term cognitive and somatic outcomes of enzyme replacement therapy in untransplanted Hurler syndrome. Mol. Genet. Metab. Rep. 2017, 13, 64–68. [Google Scholar] [CrossRef] [PubMed]
  52. Laraway, S.; Breen, C.; Mercer, J.; Jones, S.; Wraith, J.E. Does early use of enzyme replacement therapy alter the natural history of mucopolysaccharidosis I? Experience in three siblings. Mol. Genet. Metab. 2013, 109, 315–316. [Google Scholar] [CrossRef] [PubMed]
  53. Parini, R.; Deodato, F. Intravenous Enzyme Replacement Therapy in Mucopolysaccharidoses: Clinical Effectiveness and Limitations. Int. J. Mol. Sci. 2020, 21, 2975. [Google Scholar] [CrossRef] [PubMed]
  54. Tokic, V.; Barisic, I.; Huzjak, N.; Petkovic, G.; Fumic, K.; Paschke, E. Enzyme replacement therapy in two patients with an advanced severe (Hurler) phenotype of mucopolysaccharidosis I. Eur. J. Pediatr. 2006, 166, 727. [Google Scholar] [CrossRef] [PubMed]
  55. Guillén-Navarro, E.; Domingo-Jiménez, M.R.; Alcalde-Martín, C.; Cancho-Candela, R.; Couce, M.L.; Galán-Gómez, E.; Alonso-Luengo, O. Clinical manifestations in female carriers of mucopolysaccharidosis type II: A Spanish cross-sectional study. Orphanet J. Rare Dis. 2013, 8, 92. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  56. Martin, R.; Beck, M.; Eng, C.; Giugliani, R.; Harmatz, P.; Muñoz, V.; Muenzer, J. Recognition and Diagnosis of Mucopolysaccharidosis II (Hunter Syndrome). Pediatrics 2008, 121, e377. [Google Scholar] [CrossRef]
  57. Bicalho, C.G.; Rezende, M.M.; Nogueira, A.M.C.M.; Paulon, R.M.C.; Acosta, A.X. The importance of the otorhinolaryngologic evaluation in mucopolysaccharidosis patients. Int. Arch. Otorhinolaryngol. 2011, 15, 290–294. [Google Scholar] [CrossRef] [Green Version]
  58. Walker, R.; Belani, K.G.; Braunlin, E.A.; Bruce, I.A.; Hack, H.; Harmatz, P.R.; Jones, S.; Rowe, R.; Solanki, G.A.; Valdemarsson, B. Anaesthesia and airway management in mucopolysaccharidosis. J. Inherit. Metab. Dis. 2013, 36, 211–219. [Google Scholar] [CrossRef] [Green Version]
  59. Borgo, A.; Cossio, A.; Gallone, D.; Vittoria, F.; Carbone, M. Orthopaedic challenges for mucopolysaccharidoses. Ital. J. Pediatr. 2018, 44, 123. [Google Scholar] [CrossRef]
  60. Muhlebach, M.S.; Wooten, W.; Muenzer, J. Respiratory Manifestations in Mucopolysaccharidoses. Paediatric Respir. Rev. 2011, 12, 133–138. [Google Scholar] [CrossRef]
  61. Wraith, J.E.; Scarpa, M.; Beck, M.; Bodamer, O.A.; De Meirleir, L.; Guffon, N.; Meldgaard Lund, A.; Malm, G.; Van der Ploeg, A.T.; Zeman, J. Mucopolysaccharidosis type II (Hunter syndrome): A clinical review and recommendations for treatment in the era of enzyme replacement therapy. Eur. J. Pediatr. 2008, 167, 267–277. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  62. Kim, H.; An, J.Y.; Choo, O.-S.; Jang, J.H.; Park, H.Y.; Choung, Y.-H. Cochlear Implantation via the Transmeatal Approach in an Adolescent with Hunter Syndrome-Type II Mucopolysaccharidosis. J. Audiol. Otol. 2019. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  63. Bartsocas, C.; Gröbe, H.; van de Kamp, J.J.; von Figura, K.; Kresse, H.; Klein, U.; Giesberts, M.A. Sanfilippo type C disease: Clinical findings in four patients with a new variant of mucopolysaccharidosis III. Eur. J. Pediatr. 1979, 130, 251–258. [Google Scholar] [CrossRef] [PubMed]
  64. Jansen, A.C.M.; Cao, H.; Kaplan, P.; Silver, K.; Leonard, G.; De Meirleir, L.; Lissens, W.; Liebaers, I.; Veilleux, M.; Andermann, F.; et al. Sanfilippo Syndrome Type D: Natural History and Identification of 3 Novel Mutations in the GNS Gene. Arch. Neurol. 2007, 64, 1629–1634. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  65. Lin, H.-Y.; Chuang, C.-K.; Lee, C.-L.; Tu, R.-Y.; Lo, Y.-T.; Chiu, P.C.; Niu, D.-M.; Fang, Y.-Y.; Chen, T.-L.; Tsai, F.-J.; et al. Mucopolysaccharidosis III in Taiwan: Natural history, clinical and molecular characteristics of 28 patients diagnosed during a 21-year period. Am. J. Med. Genet. Part A 2018, 176, 1799–1809. [Google Scholar] [CrossRef]
  66. Zelei, T.; Csetneki, K.; Vokó, Z.; Siffel, C. Epidemiology of Sanfilippo syndrome: Results of a systematic literature review. Orphanet J. Rare Dis. 2018, 13, 53. [Google Scholar] [CrossRef] [Green Version]
  67. Ruijter, G.J.G.; Valstar, M.J.; van de Kamp, J.M.; van der Helm, R.M.; Durand, S.; van Diggelen, O.P.; Wevers, R.A.; Poorthuis, B.J.; Pshezhetsky, A.V.; Wijburg, F.A. Clinical and genetic spectrum of Sanfilippo type C (MPS IIIC) disease in The Netherlands. Mol. Genet. Metab. 2008, 93, 104–111. [Google Scholar] [CrossRef]
  68. Valstar, M.J.; Bertoli-Avella, A.M.; Wessels, M.W.; Ruijter, G.J.G.; de Graaf, B.; Olmer, R.; Elfferich, P.; Neijs, S.; Kariminejad, R.; Suheyl Ezgü, F.; et al. Mucopolysaccharidosis type IIID: 12 new patients and 15 novel mutationsb. Hum. Mutat. 2010, 31, E1348–E1360. [Google Scholar] [CrossRef]
  69. Zafeiriou, D.I.; Savvopoulou-Augoustidou, P.A.; Sewell, A.; Papadopoulou, F.; Badouraki, M.; Vargiami, E.; Gombakis, N.P.; Katzos, G.S. Serial magnetic resonance imaging findings in mucopolysaccharidosis IIIB (Sanfilippo’s syndrome B). Brain Dev. 2001, 23, 385–389. [Google Scholar] [CrossRef]
  70. Gaffke, L.; Pierzynowska, K.; Piotrowska, E.; Węgrzyn, G. How close are we to therapies for Sanfilippo disease? Metab. Brain Dis. 2018, 33, 1–10. [Google Scholar] [CrossRef] [Green Version]
  71. Lau, A.A.; Shamsani, N.J.; Winner, L.K.; Hassiotis, S.; King, B.M.; Hopwood, J.J.; Hemsley, K.M. Neonatal Bone Marrow Transplantation in MPS IIIA Mice. JIMD Rep. 2013, 8, 121–132. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  72. Sivakumur, P.; Wraith, J.E. Bone marrow transplantation in mucopolysaccharidosis type IIIA: A comparison of an early treated patient with his untreated sibling. J. Inherit. Metab. Dis. 1999, 22, 849–850. [Google Scholar] [CrossRef] [PubMed]
  73. Welling, L.; Marchal, J.P.; van Hasselt, P.; van der Ploeg, A.T.; Wijburg, F.A.; Boelens, J.J. Early Umbilical Cord Blood-Derived Stem Cell Transplantation Does Not Prevent Neurological Deterioration in Mucopolysaccharidosis Type III. JIMD Rep. 2015, 18, 63–68. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  74. Kim, K.H.; Dodsworth, C.; Paras, A.; Burton, B.K. High dose genistein aglycone therapy is safe in patients with mucopolysaccharidoses involving the central nervous system. Mol. Genet. Metab. 2013, 109, 382–385. [Google Scholar] [CrossRef]
  75. Heldermon, C.D.; Qin, E.Y.; Ohlemiller, K.K.; Herzog, E.D.; Brown, J.R.; Vogler, C.; Hou, W.; Orrock, J.L.; Crawford, B.E.; Sands, M.S. Disease correction by combined neonatal intracranial AAV and systemic lentiviral gene therapy in Sanfilippo Syndrome type B mice. Gene Ther. 2013, 20, 913–921. [Google Scholar] [CrossRef]
  76. Heldermon, C.D.; Ohlemiller, K.K.; Herzog, E.D.; Vogler, C.; Qin, E.; Wozniak, D.F.; Tan, Y.; Orrock, J.L.; Sands, M.S. Therapeutic efficacy of bone marrow transplant, intracranial AAV-mediated gene therapy, or both in the mouse model of MPS IIIB. Mol. Ther. J. Am. Soc. Gene Ther. 2010, 18, 873–880. [Google Scholar] [CrossRef]
  77. Tomatsu, S.; Montaño, A.M.; Nishioka, T.; Orii, T. Mucopolysaccharidosis IV (Morquio Syndrome; MPS IV). In Lysosomal Storage Disorders; Barranger, J.A., Cabrera-Salazar, M., Eds.; Springer US: Boston, MA, USA, 2007; pp. 433–445. ISBN 978-0-387-70909-3. [Google Scholar]
  78. Montaño, A.; Tomatsu, S.; Gottesman, G.; Smith, M.; Orii, T. International Morquio A Registry: Clinical manifestation and natural course of Morquio A disease. J. Inherit. Metab. Dis. 2007, 30, 165–174. [Google Scholar] [CrossRef]
  79. Harmatz, P.; Mengel, K.E.; Giugliani, R.; Valayannopoulos, V.; Lin, S.P.; Parini, R.; Guffon, N.; Burton, B.K.; Hendriksz, C.J.; Mitchell, J.; et al. The Morquio A Clinical Assessment Program: Baseline results illustrating progressive, multisystemic clinical impairments in Morquio A subjects. Mol. Genet. Metab. 2013, 109, 54–61. [Google Scholar] [CrossRef] [Green Version]
  80. Hendriksz, C.J.; Berger, K.I.; Giugliani, R.; Harmatz, P.; Kampmann, C.; Mackenzie, W.G.; Raiman, J.; Villarreal, M.S.; Savarirayan, R. International guidelines for the management and treatment of Morquio A syndrome. Am. J. Med. Genet. Part A 2015, 167, 11–25. [Google Scholar] [CrossRef]
  81. Hendriksz, C.J.; Harmatz, P.; Beck, M.; Jones, S.; Wood, T.; Lachman, R.; Gravance, C.G.; Orii, T.; Tomatsu, S. Review of clinical presentation and diagnosis of mucopolysaccharidosis IVA. Mol. Genet. Metab. 2013, 110, 54–64. [Google Scholar] [CrossRef] [Green Version]
  82. Arbisser, A.I.; Donnelly, K.A.; Scott, C.I.; DiFerrante, N.; Singh, J.; Stevenson, R.E.; Aylesworth, A.S.; Howell, R.R. Morquio-like syndrome with beta galactosidase deficiency and normal hexosamine sulfatase activity: Mucopolysacchariodosis IVB. Am. J. Med. Genet. 1977, 1, 195–205. [Google Scholar] [CrossRef] [PubMed]
  83. Kubaski, F.; Kecskemethy, H.H.; Harcke, H.T.; Tomatsu, S. Bone mineral density in mucopolysaccharidosis IVB. Mol. Genet. Metab. Rep. 2016, 8, 80–84. [Google Scholar] [CrossRef] [PubMed]
  84. O’Brien, J.S.; Gugler, E.; Giedion, A.; Wiessmann, U.; Herschkowitz1, N.; Meier, C.; Leroy, J. Spondyloepiphyseal dysplasia, corneal clouding, normal intelligence and acid β-galactosidase deficiency. Clin. Genet. 1976, 9, 495–504. [Google Scholar] [CrossRef] [PubMed]
  85. Hendriksz, C.J.; Santra, S.; Jones, S.A.; Geberhiwot, T.; Jesaitis, L.; Long, B.; Qi, Y.; Hawley, S.M.; Decker, C. Safety, immunogenicity, and clinical outcomes in patients with Morquio A syndrome participating in 2 sequential open-label studies of elosulfase alfa enzyme replacement therapy (MOR-002/MOR-100), representing 5 years of treatment. Mol. Genet. Metab. 2018, 123, 479–487. [Google Scholar] [CrossRef] [PubMed]
  86. Hendriksz, C.J.; Giugliani, R.; Harmatz, P.; Mengel, E.; Guffon, N.; Valayannopoulos, V.; Parini, R.; Hughes, D.; Pastores, G.M.; Lau, H.A.; et al. Multi-domain impact of elosulfase alfa in Morquio A syndrome in the pivotal phase III trial. SI Lysosome 2015, 114, 178–185. [Google Scholar] [CrossRef] [PubMed]
  87. Tomatsu, S.; Sawamoto, K.; Almeciga-Diaz, C.J.; Shimada, T.; Bober, M.B.; Chinen, Y.; Yabe, H.; Montaño, A.M.; Giugliani, R.; Kubaski, F.; et al. Impact of enzyme replacement therapy and hematopoietic stem cell transplantation in patients with Morquio A syndrome. Drug Des. Devel. Ther. 2015, 9, 1937–1953. [Google Scholar] [CrossRef] [Green Version]
  88. Hiramatsu, M.; Nakamura, K. Elosulfase alfa enzyme replacement therapy attenuates disease progression in a non-ambulatory Japanese patient with Morquio A syndrome (case report). Mol. Genet. Metab. Rep. 2017, 13, 76–79. [Google Scholar] [CrossRef]
  89. Chinen, Y.; Higa, T.; Tomatsu, S.; Suzuki, Y.; Orii, T.; Hyakuna, N. Long-term therapeutic efficacy of allogenic bone marrow transplantation in a patient with mucopolysaccharidosis IVA. Mol. Genet. Metab. Rep. 2014, 1, 31–41. [Google Scholar] [CrossRef]
  90. Yabe, H.; Tanaka, A.; Chinen, Y.; Kato, S.; Sawamoto, K.; Yasuda, E.; Shintaku, H.; Suzuki, Y.; Orii, T.; Tomatsu, S. Hematopoietic stem cell transplantation for Morquio A syndrome. Mol. Genet. Metab. 2016, 117, 84–94. [Google Scholar] [CrossRef] [Green Version]
  91. Alméciga-Díaz, C.J.; Montaño, A.M.; Tomatsu, S.; Barrera, L.A. Adeno-associated virus gene transfer in Morquio A disease—Effect of promoters and sulfatase-modifying factor 1. FEBS J. 2010, 277, 3608–3619. [Google Scholar] [CrossRef]
  92. Alméciga-Díaz, C.J.; Montaño, A.M.; Barrera, L.A.; Tomatsu, S. Tailoring the AAV2 capsid vector for bone-targeting. Pediatr. Res. 2018, 84, 545–551. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  93. Sawamoto, K.; Tomatsu, S. Development of Substrate Degradation Enzyme Therapy for Mucopolysaccharidosis IVA Murine Model. Int. J. Mol. Sci. 2019, 20, 4139. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  94. Nagao, K.; Walter, C.; Parkes, W.J.; Teixido, M.; Theroux, M.C.; Szymkowski, S.; Morlet, T.; Tomatsu, S. Cochlear implantation in a patient with mucopolysaccharidosis IVA. SAGE Open Med. Case Rep. 2019, 7, 2050313X19873791. [Google Scholar] [CrossRef] [PubMed]
  95. Giugliani, R.; Lampe, C.; Guffon, N.; Ketteridge, D.; Leao-Teles, E.; Wraith, J.E.; Jones, S.A.; Piscia-Nichols, C.; Lin, P.; Quartel, A.; et al. Natural history and galsulfase treatment in mucopolysaccharidosis VI (MPS VI, Maroteaux-Lamy syndrome)--10-year follow-up of patients who previously participated in an MPS VI Survey Study. Am. J. Med. Genet. Part A 2014, 164, 1953–1964. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  96. Akyol, M.U.; Alden, T.D.; Amartino, H.; Ashworth, J.; Belani, K.; Berger, K.I.; Borgo, A.; Braunlin, E.; Eto, Y.; Gold, J.I.; et al. Recommendations for the management of MPS VI: Systematic evidence-and consensus-based guidance. Orphanet J. Rare Dis. 2019, 14, 118. [Google Scholar] [CrossRef] [PubMed]
  97. Chintalapati, K.; Tomatsu, S.; Morlet, T.; Nagao, K. Longitudinal analysis of hearing loss in mucopolysaccharidosis types IV and VI. In Proceedings of the 10th Annual Undergraduate Research & Service Scholar Celebratory Symposium, University of Delaware, Newark, DE, USA, 15 August 2019; Available online: (accessed on 3 August 2020).
  98. Shigematsu, Y.; Hori, C.; Nakai, A.; Kuriyama, M.; Kikawa, Y.; Konishi, Y.; Sudo, M.; Konishi, K. Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome) with hearing impairment and pupillary membrane remnants. Acta Paediatrics Int. 1991, 33, 476–481. [Google Scholar] [CrossRef] [PubMed]
  99. Barone, R.; Pellico, A.; Pittalà, A.; Gasperini, S. Neurobehavioral phenotypes of neuronopathic mucopolysaccharidoses. Ital. J. Pediatr. 2018, 44, 121. [Google Scholar] [CrossRef] [Green Version]
  100. Guffon, N.; Froissart, R.; Fouilhoux, A. A rare late progression form of Sly syndrome mucopolysaccharidosis. JIMD Rep. 2019, 49, 1–6. [Google Scholar] [CrossRef] [Green Version]
  101. Sands, M.S.; Vogler, C.; Torrey, A.; Levy, B.; Gwynn, B.; Grubb, J.; Sly, W.S.; Birkenmeier, E.H. Murine mucopolysaccharidosis type VII: Long term therapeutic effects of enzyme replacement and enzyme replacement followed by bone marrow transplantation. J. Clin. Investig. 1997, 99, 1596–1605. [Google Scholar] [CrossRef] [Green Version]
  102. Sands, M.S.; Birkenmeier, E.H. A single-base-pair deletion in the beta-glucuronidase gene accounts for the phenotype of murine mucopolysaccharidosis type VII. Proc. Natl. Acad. Sci. USA 1993, 90, 6567–6571. [Google Scholar] [CrossRef] [Green Version]
  103. Cadaoas, J.; Boyle, G.; Jungles, S.; Cullen, S.; Vellard, M.; Grubb, J.H.; Jurecka, A.; Sly, W.; Kakkis, E. Vestronidase alfa: Recombinant human β-glucuronidase as an enzyme replacement therapy for MPS VII. Mol. Genet. Metab. 2020, 130, 65–76. [Google Scholar] [CrossRef] [PubMed]
  104. McCafferty, E.H.; Scott, L.J. Vestronidase Alfa: A Review in Mucopolysaccharidosis VII. BioDrugs Clin. Immunother. Biopharm. Gene Ther. 2019, 33, 233–240. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  105. Triggs-Raine, B.; Salo, T.J.; Zhang, H.; Wicklow, B.A.; Natowicz, M.R. Mutations in HYAL1, a member of a tandemly distributed multigene family encoding disparate hyaluronidase activities, cause a newly described lysosomal disorder, mucopolysaccharidosis IX. Proc. Natl. Acad. Sci. USA 1999, 96, 6296–6300. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  106. Martin, D.C.; Atmuri, V.; Hemming, R.J.; Farley, J.; Mort, J.S.; Byers, S.; Hombach-Klonisch, S.; Csoka, A.B.; Stern, R.; Triggs-Raine, B.L. A mouse model of human mucopolysaccharidosis IX exhibits osteoarthritis. Hum. Mol. Genet. 2008, 17, 1904–1915. [Google Scholar] [CrossRef]
  107. Triggs-Raine, B.; Natowicz, M.R. Biology of hyaluronan: Insights from genetic disorders of hyaluronan metabolism. World J. Biol. Chem. 2015, 6, 110–120. [Google Scholar] [CrossRef]
  108. Jadin, L.; Wu, X.; Ding, H.; Frost, G.I.; Onclinx, C.; Triggs-Raine, B.; Flamion, B. Skeletal and hematological anomalies in HYAL2-deficient mice: A second type of mucopolysaccharidosis IX? FASEB J. Off. Publ. Fed. Am. Soc. Exp. Biol. 2008, 22, 4316–4326. [Google Scholar] [CrossRef]
  109. Węgrzyn, G.; Jakóbkiewicz-Banecka, J.; Narajczyk, M.; Wiśniewski, A.; Piotrowska, E.; Gabig-Cimińska, M.; Kloska, A.; Słomińska-Wojewódzka, M.; Korzon-Burakowska, A.; Węgrzyn, A. Why are behaviors of children suffering from various neuronopathic types of mucopolysaccharidoses different? Med. Hypotheses 2010, 75, 605–609. [Google Scholar] [CrossRef] [Green Version]
  110. Bianchi, P.M.; Gaini, R.; Vitale, S. ENT and mucopolysaccharidoses. Ital. J. Pediatr. 2018, 44, 127. [Google Scholar] [CrossRef]
  111. Torres, D.A.; Barth, A.L.; Valente, M.P.M.; Mello, P.P.D.; Horovitz, D.D.G. Otolaryngologists and the Early Diagnosis of Mucopolysaccharidoses: A Cross-Sectional Study. Diagn. Basel Switz. 2019, 9, 187. [Google Scholar] [CrossRef] [Green Version]
  112. Wold, S.M.; Derkay, C.S.; Darrow, D.H.; Proud, V. Role of the pediatric otolaryngologist in diagnosis and management of children with mucopolysaccharidoses. Int. J. Pediatr. Otorhinolaryngol. 2010, 74, 27–31. [Google Scholar] [CrossRef]
Figure 1. Hearing loss pathophysiology in mucopolysaccharidoses (MPS). GAG, glycosaminoglycan; CNS, central nervous system; HL, hearing loss.
Figure 1. Hearing loss pathophysiology in mucopolysaccharidoses (MPS). GAG, glycosaminoglycan; CNS, central nervous system; HL, hearing loss.
Diagnostics 10 00554 g001
Table 1. Mucopolysaccharidoses (MPS) subtypes with enzyme deficiency and subsequent collection of glycosaminoglycans (GAGs).
Table 1. Mucopolysaccharidoses (MPS) subtypes with enzyme deficiency and subsequent collection of glycosaminoglycans (GAGs).
MPS SubtypeEnzymeGAGs
MPS I (Hurler syndrome)alpha-L-iduronidase [1]DS and HS [1]
MPS II (Hunter syndrome)iduronate-2-sulfatase [2]DS and HS [1]
MPS IIIA (Sanfilippo syndrome type A)heparan N-sulfatase [3]HS [1]
MPS IIIB (Sanfilippo syndrome type B)alpha-N-acetylglucosaminidase [3]HS [1]
MPS IIIC (Sanfilippo syndrome type C)acetyl CoA alpha-glucosaminide acetyltransferase [3]HS [1]
MPS IIID (Sanfilippo syndrome type D)N-acetylglucosamine 6-sulfatase [3]HS [1]
MPS IVA (Morquio syndrome type A)N-acetylgalactosamine-6-sulfate sulfatase [4]Chondroitin-6-sulfate and KS [4]
MPS IV B (Morquio syndrome type B)beta-galactosidase [5]KS [5]
MPS VI (Maroteaux–Lamy syndrome)arylsulfatase B [6]DS [1]
MPS VII (Sly syndrome)glucuronidase [1]Chondroitin sulfate, DS, and HS [1]
MPS IX (Natowicz syndrome)hyaluronidase [7]Hyaluronic acid [7]
DS = dermatan sulfate; HS = heparan sulfate; KS = keratan sulfate.
Table 2. Summary of studies on auditory characteristics of MPS.
Table 2. Summary of studies on auditory characteristics of MPS.
SourceMPS Type(s)Article Type
(Research, Case Study, Review)
Simmons et al., 2005 [9]All MPS typesRetrospective reviewN/AHuman
Silveira et al., 2018 [10]I, II, III, IV, VIDescriptive, cross-sectional study53Human
Lenka et al., 2020 [11]I, II, III, IV, VIRetrospective review61Human
Ahn et al., 2019 [12]I, II, III, IV, VIRetrospective review124Human
Mesolella et al., 2013 [13]I, II, III, IV, VIObservational Study20Human
Lin et al., 2014 [14]I, II, IV, VIClinical study39Human
Vargas-Gamarra et al., 2017 [15]I, II, III, IVRetrospective study23Human
Gokdogan et al., 2016 [16]I, III, IV, VIClinical study9Human
Giraldo et al., 2020 [17]II, IVA, VIRetrospective study35Human
Da Costa et al., 2012 [18]I, IIRetrospective study30Human
van den Broek et al., 2020 [19]I, VIRetrospective study32Human
Aldenhoven et al., 2015 [20]IRetrospective study217Human
Dualibi et al., 2016 [21]IProspective study9Human
Kiely et al., 2017 [22]IRetrospective review55Human
Friedmann et al., 1985 [23]IHistopathological study2Human
Kariya et al., 2012 [24]ITemporal bone scan study6Human
Souillet et al., 2003 [25]IProspective study27Human
Schachern et al., 2007 [26]IResearch studyN/AMouse
Schachern et al., 1984 [27]ITemporal bone scan study3Human
Keilmann et al., 2012 [28]IISurvey/Registry554Human
Chiong et al., 2017 [29]IICase series23Human
Muenzer et al., 2006 [30]IIClinical trial96Human
Hong et al., 2012 [31]IIResearch studyN/AMouse
Buhrman et al. 2014 [32]IIIARetrospective review46Human
Heldermon et al., 2007 [33]IIIBResearch studyN/AMouse
Nagao et al., 2018 [34]IVA, IVBClinical study14Human
Riedner and Levin, 1977 [35]IVAudiological/Otologic review21Human
Swartz and Santi, 1997 [36]IVAnimal researchN/AAnimal (chinchilla, cat, gerbil, rabbit)
Gomes et al., 2019 [37]VIClinical review362Human
Furujo et al., 2017 [38]VICase study2Human
Harmatz et al., 2014 [39]VIClinical trial reviewN/AHuman
Horovitz et al., 2013 [40]VIRetrospective review34Human
Montaño et al., 2016 [41]VIISurvey56Human
Ohlemiller et al., 2002 [42]VIIResearch studyN/AMouse
O’Connor et al., 1998 [43]VIIResearch studyN/AMouse
Sands et al., 1995 [44]VIIResearch studyN/AMouse
Berry et al., 1994 [45]VIIResearch studyN/AMouse
Natowicz et al., 1996 [7]IXCase report1Human
Imundo et al., 2011 [46]IXClinical case reports3Human
Table 3. Genes and affected enzymes of MPS III.
Table 3. Genes and affected enzymes of MPS III.
TypeEnzymeOMIM NumberGene
MPS IIIAHeparan N-sulfatase252900SGSH
MPS IIIBAlpha-N-acetylglucosaminidase252920NAGLU
MPS IIICAcetyl CoA alpha-glucosaminide acetyltransferase252930HGSNAT
MPS IIIDN-acetylglucosamine 6-sulfatase252940GNS

Share and Cite

MDPI and ACS Style

Wolfberg, J.; Chintalapati, K.; Tomatsu, S.; Nagao, K. Hearing Loss in Mucopolysaccharidoses: Current Knowledge and Future Directions. Diagnostics 2020, 10, 554.

AMA Style

Wolfberg J, Chintalapati K, Tomatsu S, Nagao K. Hearing Loss in Mucopolysaccharidoses: Current Knowledge and Future Directions. Diagnostics. 2020; 10(8):554.

Chicago/Turabian Style

Wolfberg, Jeremy, Keerthana Chintalapati, Shunji Tomatsu, and Kyoko Nagao. 2020. "Hearing Loss in Mucopolysaccharidoses: Current Knowledge and Future Directions" Diagnostics 10, no. 8: 554.

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop