The Diagnostic Journey of a Patient with Prader–Willi-Like Syndrome and a Unique Homozygous SNURF-SNRPN Variant; Bio-Molecular Analysis and Review of the Literature

Prader–Willi syndrome (PWS) is a rare genetic condition characterized by hypotonia, intellectual disability, and hypothalamic dysfunction, causing pituitary hormone deficiencies and hyperphagia, ultimately leading to obesity. PWS is most often caused by the loss of expression of a cluster of genes on chromosome 15q11.2-13. Patients with Prader–Willi-like syndrome (PWLS) display features of the PWS phenotype without a classical PWS genetic defect. We describe a 46-year-old patient with PWLS, including hypotonia, intellectual disability, hyperphagia, and pituitary hormone deficiencies. Routine genetic tests for PWS were normal, but a homozygous missense variant NM_003097.3(SNRPN):c.193C>T, p.(Arg65Trp) was identified. Single nucleotide polymorphism array showed several large regions of homozygosity, caused by high-grade consanguinity between the parents. Our functional analysis, the ‘Pipeline for Rapid in silico, in vivo, in vitro Screening of Mutations’ (PRiSM) screen, showed that overexpression of SNRPN-p.Arg65Trp had a dominant negative effect, strongly suggesting pathogenicity. However, it could not be confirmed that the variant was responsible for the phenotype of the patient. In conclusion, we present a unique homozygous missense variant in SNURF-SNRPN in a patient with PWLS. We describe the diagnostic trajectory of this patient and the possible contributors to her phenotype in light of the current literature on the genotype–phenotype relationship in PWS.


Introduction
Prader-Willi syndrome (PWS) is a rare genetic condition (estimated prevalence of 1:10,000-1:30,000), affecting multiple organ systems [1]. In the neonatal period, PWS is characterized by muscular hypotonia and feeding difficulties, which usually require tube feeding. Later in infancy, patients switch to hyperphagia (overeating) due to abnormal satiety response to food intake [1][2][3]. Endocrine features include growth hormone deficiency, hypothyroidism, hypogonadism, and, rarely, central adrenal insufficiency [1,3,4]. Both hyperphagia and pituitary dysfunction contribute to abnormal weight gain, which can ultimately lead to obesity. Additionally, temperature regulation and pain registration are often disturbed [1,2,5]. The majority of these features can be explained by hypothalamic dysfunction [6]. Moreover, patients with PWS often display developmental delay, autism spectrum disorders (ASD), ASD-like behavior [1,7], and challenging behavior [3]. The physical appearance is characterized by short stature, obesity, almond-shaped eyes, strabismus, small bitemporal diameter, a thin upper lip, small hands and feet, and tapering fingers [1,3]. Commonly used consensus diagnostic criteria are those proposed by Holm et al. [8] in 1993 (Table 1). Total points index case 10 points

Requirements clinical diagnosis PWS for adults 8 points, of which 5 points major
Major criteria are weighted at one point each and minor criteria at half a point each. For adults, a total score of eight, of which at least five points for the major criteria, is necessary for the clinical diagnosis of PWS [8].
PWS is usually caused by the absence of expression of a cluster of paternally expressed genes on chromosome 15q11.2-q13. The maternal allele is imprinted, and therefore genomic and epigenetic changes lead to PWS only if they occur in the paternally expressed genes. PWS is most commonly caused by a paternal deletion (70-75%), a uniparental maternal disomy 15 (mUPD, 25-30%), an imprinting center defect (ICD, 1-3%), or a paternal chromosomal translocation (rare) [9,10]. The so called 'Prader-Willi syndrome critical region' on chromosome 15q11.2-q13 encompasses several genes, including MKRN3, MAGEL2, NDN, NPAP1, SNURF-SNRPN, and numerous non-coding RNAs (ncRNAs) including small nucleolar RNAs (snoRNAs) [10]. The exact function of most of these genes and their exact relation to the PWS phenotype still remains unclear.
In patients with Prader-Willi-like syndrome (PWLS), PWS features are present without the classical PWS genotype (paternal deletion, mUPD, ICD, or translocation of chromosome 15q11. [2][3][4][5][6][7][8][9][10][11][12][13]. To provide adequate treatment and genetic counselling to the patients with PWLS and their relatives, it is important to understand the underlying genetic defects and pathways [10]. Cases with PWLS provide novel insight into the complex genotypephenotype relationship of PWS. Many chromosomal alterations involving different chromosomes have been described in relation to PWLS [10][11][12]. Several cases of PWLS with a small deletion in the PWS critical region have been described. Deletions ranged from 80 to 236 kb and most include SNORD116 and the 'imprinted in Prader-Willi syndrome' (IPW) gene [13][14][15][16][17][18][19]. These case reports suggest that the region encoding SNORD116 and IPW is responsible for the key characteristics of PWS, while other genes in the PWS critical region may have smaller phenotypic contributions.
We now present a patient with PWLS, with a normal result on genetic diagnostic testing for PWS, without abnormalities in SNORD116 or IPW. We describe the fascinating diagnostic trajectory and discuss possible explanations for her phenotype in light of the current knowledge on the genotype-phenotype relationship in PWS.

Materials and Methods
The patient and her mother, who is legal representative, gave permission for the use of the clinical information and pictures in the current paper.

Single Nucleotide Polymorphism (SNP) Array
Genomic DNA was extracted from peripheral blood and hybridized to a Human CytoSNP-12 array (Illumina, San Diego, CA, USA) as reported before [21]. The array was scanned with the Illumina iScan Control. Data were processed using Genome Studio v2.1 software and analyzed with Nexus Copy Number software v5.0 (Biodiscovery, El Segundo, CA, USA).

Next Generation Sequencing (NSG)
Obesity gene panel sequencing was performed at the genetic diagnostics laboratory of the UMC Utrecht to search for pathogenic abnormalities in the exons of 57 protein coding obesity-associated genes, as described previously [22]. Identified variants were classified according to the American College of Medical Genetics and Genomics guidelines for variant classification.

RNA Sequencing
A punch biopsy of the skin was taken from the index case and the mother. RNA sequencing was performed at the Institute of Human Genetics, University Hospital Essen. In order to understand whether, and how, the new variant affects gene expression, we compared RNA sequencing data from the patient and her mother to healthy controls and patients with genetically confirmed classical PWS.

PRiSM Screen
We assessed the effect of the SNRPN variant on protein function and its pathogenicity using our in-house developed functional genomics screen "Pipeline for Rapid in silico, in vivo, in vitro Screening of Mutations (PRiSM)" (for other studies where this has been used see [29][30][31][32]).

Constructs
To obtain the cDNA sequence from human SNRPN (NM_003097.6) a PCR (Phusion high fidelity, Thermo Fisher) was done on the human brain cDNA library, using the following primers: Fw 5 GGCGCGCCACCATGACTGTTGGCAAGAGTAG 3 and Rev 5 TTAATTAACTAAGGTCTTGGTGGACG 3 . The gene was then cloned into our dual promoter expression vector [31][32][33]. Using PCR (Phusion high fidelity, Thermo Fisher) we then introduced the single nucleotide variant using the following primers: SNRPNc.193c>t (p.Arg65Trp), Fw 5 CCAGAGCGTGAAGAAAAGTGGGTTTTGGGTCTGGTGT 3 and Rev 5 ACAC-CAGACCCAAAACCCACTTTTCTTCACGCTCTGG 3 . The same expression vector without an inserted gene was used as control for all the in vivo and in vitro experiments (control vector).
At least 10 confocal images (20× objective, 0.5 zoom, 1024 × 1024 pixels) of different transfected neurons (identified by the red staining from the tdTomato) were obtained from each condition, with at least two independent experimental replications. Total neurite length and arborization (the number of branching of each primary neurite) was analyzed, using the NeuronJ plugin of ImageJ. All values were normalized against the mean values of the empty vector control. Analysis was done by an experimenter blinded for the transfection conditions.

In Utero Electroporation
The in utero electroporation was done as described previously [32]. In short, pregnant FvB/NHsD mice at E14.5 of gestation were anesthetized, and the uterus was exposed. Through the uterus wall, the DNA construct (1.5-3 µg/µL, diluted in fast green (0.05%)) was injected in the lateral ventricle of the embryos, using a glass pipette controlled by a Picospritzer ® III device. Using tweezer-type electrodes connected to a pulse generator (ECM 830, BTX Harvard Apparatus), five electrical square pulses of 45 V (50 ms per pulse and 150 ms inter-pulse interval (ipi)) were delivered. The positive pole of the tweezers was placed on top of the developing somatosensory cortex. Plasmids injected: empty vector control, SNRPN-WT, or SNRPN-p.Arg65Trp. After birth, pups (M/F) were sacrificed at P1 for histochemical processing.

Statistical Analysis
We assumed normally distributed data. For the in vitro and in vivo overexpression experiments, statistical difference was determined using one-way analysis of variance (ANOVA) followed by Dunnett's post-hoc test for multiple comparisons. Two-tailed unpaired t-test (dual comparison) was used for the Western blot analysis. We analyzed neuronal migration based on the proportion of electroporated cells that migrated to the cortical plate at P1 (defined as the most proximal 40% of dorsoventral distance between the pia and ventricle (first four of ten equally spaced bins)).

Literature Review
We performed a search on Embase, Medline, the Web of Science Core Collection, Cochrane Central Register of Controlled Trials, and Google Scholar for case reports of patients with genetic alterations (e.g., translocations, deletions, genetic variants) in the PWS critical region on the paternal chromosome that affected only part of the PWS critical region. We included case reports and case series that provide a description of the genotype and phenotype of each individual case. We included articles about patients with and without features of PWS. Exclusion criteria were articles that were not available online, articles that were not available in English, patients with genetic alterations of the PWS critical region on the maternal chromosome only, case reports where the entire PWS critical region or the PWS-imprinting center (IC) was affected, case reports where the affected region extended beyond the PWS critical region, and case reports with insufficient genotyping or phenotyping. For the full search strategy, see Table S2.

Patient Description
The female patient presented at our hospital at the age of 46 years, after she had been referred for treatment of morbid-obesity. She fulfilled the criteria for the clinical diagnosis of PWS, as is shown in Table 1.

Medical History
There were little fetal movements during pregnancy. The index case was born after a pregnancy of 40 weeks with a birth weight of three kilograms (−0.5 SD). Postnatally, she was cyanotic and hypotonic. Her neonatal feeding difficulties required tube feeding for which she was hospitalized for several months. Her feeding difficulties persisted until she was 1.5 years old, after which she developed hyperphagia, resulting in obesity at the age of four. When she was twelve years old, her weight was 125 kg according to her mother. Secondary to her obesity, she had developed type 2 diabetes mellitus and dyslipidaemia, for which she was treated with metformin and simvastatin, respectively. Psychomotor development was severely delayed; she started walking at the age of eight years and talking at the age of 40 years. She received special education. She had primary amenorrhea.

Anamnesis
The patient had clear hyperphagia: She could easily eat four full plates of food. Her mother, who was the primary caregiver, reported challenging behavior including temper tantrums, stealing food, skin picking, and trichotillomania.

Family History
The parents of the index case were first-degree relatives. The mother of the index case had many (half-) siblings, of which most were illiterate or had great difficulty reading and writing, mainly caused by lack of education during childhood. Although both the mother of the index case and multiple siblings had short stature and were overweight, none of the family members had the same phenotype as the index case. However, the mother had lost contact with most relatives and, therefore, family health history was incomplete.
The mother of the patient was 157 cm tall and weighed 91 kg (body mass index (BMI) 37 kg/m 2 ).

Physical Examination
Physical examination revealed a typical PWS appearance of the index case, with obesity (BMI 34 kg/m 2 ), hypotonia, kyphosis, high-arched feet (requiring orthopedic shoes), and small hands with tapering fingers. Facial features included narrow bitemporal diameter, almond-shaped eyes, and strabismus ( Figure 1). She had some breast formation, but exact Tanner stage for breast development was hard to assess due to her obesity. She had Tanner stage 3 pubic hair development. Her height was 158 cm (−2 SD, [35]), her weight 85 kg, and her head circumference 56.5 cm (+0.7 SD).

Biochemistry and Imaging
Laboratory results revealed central hypogonadism and a lowered Insulin-like growth factor (IGF)1 level (Table S1). Peak growth hormone value during growth hormone releasing hormone (GHRH) and arginine stimulation test was 2.9 µg/L. This is lower than the cut-off of 4.2 µg/L in obese subjects [36], confirming the diagnosis growth hormone deficiency. Cortisol and thyroid hormone levels were normal. Dual-energy X-ray absorptiometry (DEXA) scan showed osteopenia of the lumbar vertebrae and osteoporosis of the femoral neck.

Polysomnography
Polysomnography showed mild sleep apnea with an apnea-hypopnea index of 6.2 per hour [37].

Features Not Corresponding to PWS
Apart from the typical PWS features, the patient also had features not corresponding to PWS, like celiac disease, tinnitus, hearing loss (requiring a hearing aid), cataract (requiring lens implantation), and arthralgia of the hands and feet. Atypical findings during physical examination were a remarkable overbite, diastemata, multiple naevi, and a small palpebral fissure width. Her relatively tall stature (158 cm, while most PWS females have a height below 150 cm) was also atypical for PWS. Additionally, MRI of the brain also revealed abnormalities not specific for PWS, including septo-optic dysplasia (SOD), with several midline defects, including partial agenesis of the corpus callosum and the septum pellucidum and an atrophic left optic nerve, but the pituitary gland had a normal size [38]. In addition, there was partial agenesis of the sagittal sinus and most likely agenesis of the falx cerebri. Lastly, there was a small lesion in the left-posterior part of the pituitary gland with a maximum diameter of 5 mm, most likely a pituitary incidentaloma. Her clinical, behavioral, and dysmorphic features are shown in Table 2. As the patient fulfilled the consensus criteria for Prader-Willi syndrome (Table 1), we performed genetic diagnostic testing for PWS. After routine PWS methylation tests, using methylation-specific multiplex-ligation probe amplification (MS-MLPA), ruled out the presence of a deletion, mUPD, or ICD of chromosome 15q11.  [22]. The mother was heterozygous for the same variant. The father was not available for DNA analysis. Hemizygosity in the index patient was excluded by MS-MLPA analysis. Single nucleotide polymorphism array (SNP) array showed several large regions of homozygosity (ROH), caused by high-grade consanguinity between the parents (Figure 3). The exact coordinates of the breakpoints can be found in Table S3.
SNURF-SNRPN was located in one of the ROH. In silico analysis using variant effect predictor programs Align-GVGD [23], MutationTaster (Build NCBI37/Ensembl 69) [24], sorting intolerant from tolerant (SIFT) [25,26], and Polymorphism Phenotyping v2 (Polyphen-2) [27,28] predicted that NM_003097.3(SNRPN):c.193C>T, p.(Arg65Trp) is deleterious. The variant was not present in the 1000 Genomes Project (Phase 3 release) [42] or in the genome aggregation database (gnomAD v2.1.1) [43]. The protein structure of SNRPN and the location of the changed amino acid is depicted in Figure 4. RNA sequencing analysis showed equal expression of SNRPN and all other genes in the PWS critical region for the index case, the mother, and four healthy, Caucasian volunteers (one male and three females) that served as controls. RNA sequencing confirmed that the mother of the patient had the variant on her paternal chromosome 15.

Literature Review
To interpret our findings in the light of the available literature, we performed a thorough literature search for case reports or case series of patients with genetic alterations (e.g., translocations, deletions, genetic variants) in the PWS critical region on the paternal chromosome that affected only part of the PWS critical region. After deduplication, we found 4693 articles, of which the titles and abstracts were reviewed. After full-text screening, we included 22 cases with PWLS. Additionally, we found 29 case reports that described abnormalities in only MAGEL2 (associated with Schaaf-Yang syndrome) and 42 case reports with abnormalities in only MKRN3 (associated with central precocious puberty), which are not included in the table. Most of the 22 cases with PWLS had a translocation or a deletion, leading to a loss of function of one or more genes of the PWS critical region. Additionally, we found one case report of a patient with a small duplication in exon 1 of SNURF, which introduced a premature stop codon in SNURF. The results of this literature review are summarized in Table 3 and Figure 6.

Discussion
We here present the puzzling diagnostic trajectory of a 46-year-old female patient with PWLS. After genetic testing excluded the classical PWS genetic defects (deletion, mUPD, ICD, or translocation of chromosome 15q11.2-13), we performed additional genetic analyses. Obesity gene panel analysis of 57 obesity-associated genes revealed a homozygous variant NM_003097.3(SNRPN):c.193C>T, p.(Arg65Trp) in exon 6 of the SNURF-SNRPN gene, changing CGG into TGG (Figure 2). This variant was not present in the 1000 Genomes Project (Phase 3 release) [42] or in the genome aggregation database (gnomAD v2.1.1) [43]. The variant changes the non-aromatic and positively charged arginine into the aromatic, non-polar tryptophan (Arg65Trp), which is deleterious according to various variant effect predictor programs. The fact that this homozygous missense variant is located in the PWS critical region suggests a relation with the PWS phenotype of the patient.
While the patient's phenotype included PWS features, she also had atypical features, including brain lesions at MRI. Although morphological abnormalities in the brain of patients with PWS have been described [67][68][69][70][71], the brain lesions found in our patient were atypical for PWS. SNP array analysis showed multiple large ROH spread across different chromosomes, suggesting that (multiple) autosomal recessive diagnoses could contribute to the complete phenotype in this patient. Additionally, the fact that the mother of the patient had the same variant on her paternal chromosome 15 without having PWLS (she had obesity but did not fulfil any other diagnostic criteria for PWS), suggests that this variant is probably not the only explanation for the phenotype of the index case.
As she had dysgenesis of midline brain structures and optic nerve hypoplasia at MRI with hypothalamic-pituitary dysfunction [38], she fulfilled the criteria for SOD. SOD has a wide variability of clinical features, including some features that were present in our patient, like developmental delay [72], dysmorphic features, and autism-like behavior [73]. However, our patient also had many symptoms not associated with SOD, including hyperphagia, hypotonia, and kyphosis. Although the etiology remains unclear in most cases, SOD has been associated with pathogenic variants in HESX1, OTX2, SOX2, and SOX3 [38,74,75]. One of the ROH of the index patient included SOX3, but none of the ROH included HESX1, OTX2, or SOX2.
The index case has a remarkable family history with a large pedigree. Most family members were short, overweight, and/or illiterate. The latter is remarkable in the context of 10% inadequate literacy in the total Dutch 16-65 year old population [76]. The high prevalence of short stature, obesity and/or illiteracy in this family is suggestive of a genetic component. Unfortunately, other family members were unavailable for genetic analysis.
Interestingly, SNURF-SNRPN is a bi-cistronic gene, which is transcribed exclusively from the paternally inherited chromosome. SNURF-SNRPN is expressed in several tissues and shows the highest RNA expression in the brain and heart, followed by endocrine tissues, male reproductive tissues, and blood [77]. SNURF-SNRPN encodes two proteins: SNURF and SNRPN (also called SmN) [78]. The function of SNURF is unknown [78]. SNRPN is involved in mRNA splicing and predominantly expressed in neurons, especially in central neurons [79][80][81]. SNRPN influences neurite outgrowth, neuron migration, and distribution of dendritic spines in mice [82]. However, the precise role of SNRPN in the development of the PWS phenotype remains largely unknown. Apart from encoding SNURF and SNRPN proteins, SNURF-SNRPN transcription is necessary for production of downstream ncRNAs implicated in many PWS traits [83,84].
Imprinting at 15q11.2-13 is regulated by a bipartite imprinting center defined as the smaller regions of overlap (SRO) found in patients with imprinting defects [85][86][87][88][89][90]. The Angelman syndrome-SRO (AS-SRO) functions to silence paternally expressed genes on the maternal allele. The PWS-SRO functions somatically to activate paternally expressed genes on the paternal allele [91][92][93]. The PWS-SRO spans SNURF-SNRPN exon 1 [94,95]. The missense variant in this patient is in exon 6, about 20 kb downstream of the PWS-SRO and is therefore very unlikely to generate an ICD. Additionally, in our patient, imprinting and expression of the genes in the PWS critical region was normal, excluding an ICD.
The PWS critical region encompasses several genes, including MKRN3, MAGEL2, NDN, SNURF-SNRPN, and ncRNAs including snoRNAs like SNORD115 and SNORD116 [10]. Two individuals with deletions of MKRN3, MAGEL2, and NDN have been described [60,64]. These patients lacked many typical PWS features, suggesting that deletions of these genes cannot cause the full PWS phenotype on their own. However, patients with a heterozygous truncating pathogenic variant in the paternally derived allele of the MAGEL2 gene have Schaaf-Yang syndrome, which has clinical overlap with PWS, including intellectual disability, autism spectrum disorder, neonatal hypotonia, and infantile feeding problems [96,97]. Patients with Schaaf-Yang syndrome also display non-PWS features, for example distal joint contractures. SNORD115 is unlikely to play a role in the PWS phenotype, as individuals with a paternally inherited deletion of SNORD115 do not have PWS features [47,48,56,57]. SNORD116 is suspected to be a strong contributor to the PWS phenotype [98]. Several cases with PWS features and microdeletions or translocations resulting in lack of expression of SNORD116 and IPW indicate an important role of SNORD116 and IPW [13][14][15][16][17][18][19][49][50][51][52][53]58,66], Table 3. However, IPW is a non-protein coding RNA, which is minimally conserved between human and mouse genomes [99,100]. Mice with a targeted deletion of SNORD116 show cognitive deficits, abnormal growth and feeding [101,102], while mice with paternal deletions of portions of SNURF or SNRPN seem to have a normal phenotype [103,104]. It has been suggested that individuals with translocations have a milder phenotype when only SNORD116 is affected, compared to individuals in whom SNURF-SNRPN expression is also abolished. SNORD116 deletions seem to cause most of the major features of PWS, but they may be less prominent [58]. It should be noted that this is hard to investigate as all patients are assessed by different physicians, making it hard to objectively assess patients [84]. Lastly, SNURF could contribute to the PWS phenotype, as is demonstrated by Naik et al. [61], who presented a case with a small duplication in exon 1 of SNURF-SNRPN, which is predicted to only affect SNURF expression, although it cannot be ruled out that SNRPN is also affected. This patient had developmental delay, challenging behavior, and increased appetite, but also tall stature (170 cm (+3.26 SD)) and a large head circumference (57 cm (+2.69 SD)), which are not PWS features and were also not present in the index case that we present.
SNORD116 is produced from the same primary transcript as SNURF-SNRPN [83,84] and therefore variants in SNURF-SNRPN could cause a PWS phenotype through a change of expression of SNORD116. However, the RNA sequencing in our patient showed a normal expression of SNORD116. This rules out that the PWLS was caused by lack of SNORD116 expression.
PWS is generally thought to result from loss of expression of the paternal genes on the PWS critical region, as the maternal PWS critical region is imprinted and therefore not expressed. The mother of the index case had the same variant as the index case on her paternal chromosome 15. She did not have a documented intellectual disability or specific PWS features, but she was illiterate and had obesity. This suggests that the SNRPN-p.Arg65Trp variant might not always be pathogenic (incomplete penetrance) or might result in a mild phenotype. There is some evidence from mice that expression of the maternal allele of chromosome 15q11.2-13 can be detected when the paternal allele is not active [105,106]. However, findings in mice are poor predictors of the human situation and therefore the loss of silencing found by Rieusset et al. [105] cannot be extrapolated to humans.
A previous report by Iourov et al. [107] suggested that homozygosity (without mUPD) of part of 15q11.2 could be related to a mild PWLS phenotype, mainly characterized by developmental delay and/or intellectual disability. According to SNP array, homozygosity of 15q11.2 was also present in our patient and could have influenced her phenotype. However, the phenotype of our index case was specific to PWS, whereas the five cases described by Iourov et al. lacked most major phenotypic features of PWS. They did not present hypothalamic dysfunction leading to hyperphagia, pituitary hormone deficiencies, abnormal temperature regulation, or inadequate pain registration.
In our patient, RNA sequencing showed that expression of SNURF-SNRPN and the other genes in the PWS critical region were not affected. However, the change from arginine to tryptophan caused by the homozygous SNRPN variant was predicted to severely affect protein function. In order to understand whether the variant found in this patient indeed is pathogenic and whether it causes a loss of function or a gain of function, we made use of the unbiased functional genomics screen PRiSM. This showed that the variant does not cause protein instability, nor behaves differently from SNRPN-WT in the migration assay. However, whereas overexpression of SNRPN-WT resulted in a small but non-significant trend in reduced neural development in vitro, SNRPN-p.Arg65Trp significantly reduced neural development upon overexpression primary hippocampal neurons. This suggests that the missense variant might alter the function of SNRPN, causing a dominant negative effect on neuronal maturation when overexpressed. These results show that this variant does not cause a loss of function, rather it might suggest that it causes a gain of function. However, future studies are needed to confirm its functional impact.
The SNRPB'/B genes encode the proteins small nuclear ribonucleoprotein-associated polypeptide B' and B (SmB'/B). They are closely related to SNRPN, which encodes the protein SNRPN, also called small nuclear ribonucleoprotein-associated polypeptide N (SmN). Normally, SNRPN replaces SmB'/B in the brain. It has been demonstrated that the loss of SNRPN in PWS brain tissue causes a compensatory feedback loop that drastically upregulates the levels of SmB'/B. It has been suggested that upregulation of SmB'/B in PWS reduces the severity of the syndrome [108]. However, in the presence of a non-functional SNRPN protein, this compensation mechanism might not be induced, leading to more severe phenotypic features compared to cases where SNRPN is completely absent. RNA sequencing in this patient showed that SNRPB'/B expression in fibroblasts was normal.

Conclusions
In conclusion, the finding of this homozygous missense SNURF-SNRPN variant in a patient with virtually all clinical features of PWS suggests that this variant might have caused her PWLS with combined pituitary hormone deficiency (CPHD). Additionally, functional analysis suggested that the variant might affect the function of SNRPN. However, the large ROHs that were found throughout the genome suggests other autosomal recessive conditions that could contribute to her complete phenotype. The fascinating trajectory of genetic and functional analyses performed in this patient shows that the finding of a unique variant in the PWS critical region, in a patient with PWLS, does not necessarily prove a causal relationship between the two.

Informed Consent Statement:
Written informed consent has been obtained from the patient to publish this paper. Data Availability Statement: Not applicable.