2. Materials and Methods
This review was conducted as a scoping study in accordance with the methodological guidance proposed by the Joanna Briggs Institute (JBI) and reported following the PRISMA-ScR (Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews) checklist [
17,
18,
19] (
Supplementary Materials). It was prepared according to the following scheme: (1) defining inclusion and exclusion criteria, (2) developing a search strategy and adapting queries to the specifics of individual databases and search engines, (3) searching leading bibliographic databases and available grey literature sources, (4) deduplication of identified records, (5) selecting studies that met the established criteria, (6) extracting and organizing data from included studies, (7) synthesizing the results in tabular and descriptive formats, and (8) presenting the main observations and conclusions resulting from the mapping of available evidence. This scoping review was prospectively registered in the Open Science Framework (OSF) on 19 February 2026 (osf.io/tsez2) [
20].
Inclusion and exclusion criteria were developed according to the PCC(COSTL) approach and were determined before the literature search began (
Table 1) [
21]. Studies including patients diagnosed with NSD, regardless of age, were included in the review. Studies exclusively focusing on patients with genetic syndromes or congenital craniofacial defects (e.g., craniofacial syndromes) were excluded, as were studies using animal models, cadaveric materials, and in vitro studies. Publications assessing the relationship between NSD and craniofacial morphology, specifically maxillary, mandibular, and palate parameters, facial asymmetry, or malocclusion were eligible for analysis. Publications regarding sinonasal conditions affecting craniofacial morphology were excluded. NSD was required to be assessed using a specific classification system (e.g., Mladina classification) or measurable quantitative parameters (angular, linear, or volumetric). Studies that examined NSD solely in the context of ENT symptoms (e.g., nasal obstruction, sinusitis) without assessing skeletal or dentofacial parameters were excluded. Studies conducted in clinical or academic settings using radiological imaging methods such as computed tomography (CT), cone beam computed tomography (CBCT), or cephalometry were included. Studies that were purely technical or simulation-based and not based on clinical data were excluded. All study designs reporting original data were eligible for inclusion, including observational studies (cross-sectional, cohort, case–control), case series, case reports, and academic theses or dissertations. No restriction was applied regarding prospective or retrospective design. Narrative reviews, commentaries, letters to the editor, and conference abstracts without accessible full text were excluded.
The search was not restricted by language or time period, in order to reflect the current state of knowledge as broadly as possible. Search strategy was also validated on previously known relevant papers identified during the initial literature review and literature review. The final search was conducted on 28 February 2026.
To maintain the conceptual focus of this scoping review, eligible studies were required to analyze an NSD classification, morphological deviation category, severity grade, or standardized NSD assessment method as the primary exposure or stratification variable in relation to quantitative craniofacial, maxillary, mandibular, palatal, dentofacial, or asymmetry-related morphometric outcomes. Studies were excluded when NSD was reported only as presence or prevalence within predefined malocclusion, sinonasal, airway, or disease groups, when NSD was assessed only as a secondary sinonasal finding, when no quantitative craniofacial or dentofacial morphometric outcome was analyzed in relation to the NSD assessment method or when postoperative or treatment-induced changes in NSD were evaluated.
The Mladina classification was considered one of the predefined NSD classification systems of interest, but it was not used as the sole eligibility criterion.
2.1. Search Strategy and Information Sources
The search strategy was developed to identify as broadly as possible publications concerning the relationship between NSD and craniofacial morphology. Its basic structure included terms related to NSD and terms describing craniofacial morphology, facial asymmetry, maxilla, mandible, palate, and malocclusion.
The queries were then individually tailored to the specifics of each database and search engine, taking into account their different syntactic requirements and search capabilities. The search was conducted in the following databases and search engines: Bielefeld Academic Search Engine (BASE; over 400,000,000 records), The Cochrane Library (over 2,000,000 records), Embase (over 50,000,000 records), PubMed (over 40,000,000 citations), and Google Scholar (over 600,000,000 records). In order to obtain the most complete picture of the available literature, no filters were used to limit search results by language, publication date, or document type. Google Scholar searches were conducted using the “allintitle:” operator to increase the specificity and reproducibility of results. This limited the search to records containing key terms in the title and reduced the number of results that were not directly related to the topic.
2.2. Selection Process
Identified records were first manually deduplicated using the Rayyan tool (version 2026-03-01, Qatar Computing Research Institute, Doha, Qatar and Rayyan Systems, Cambridge, MA, USA). Two independent, blinded researchers (J.W. and M.K.) then performed an initial assessment of publication eligibility based on titles and abstracts. In case of discrepancies, the record was forwarded to the full-text review stage. Full-text analysis was also independently conducted by the same two researchers (J.W. and M.K.), and in cases of disagreement, the final decision was made by a third researcher (F.B.).
2.3. Data Collection Process
Data extraction was performed independently by two investigators (J.W. and M.K.) based on full-text analysis of included studies. Primary outcomes were quantitative skeletal, asymmetry, or dentofacial measures reported in association with NSD. These included maxillary, mandibular, palatal, transverse craniofacial, facial asymmetry, malocclusion, and nasal volume parameters. Secondary outcomes included the method used to assess NSD, such as the Mladina classification, other classifications, angular or linear measurements, volumetric assessment, or imaging-based severity assessment. The direction of the reported association between NSD and each extracted morphological outcome was also recorded. Additional data extracted from eligible publications included author, year of publication, country, study design, sample size, age of participants, study setting, imaging method, inclusion and exclusion criteria, comparison groups, statistical methods, main findings, and limitations reported by the original authors. In case of discrepancy between the two investigators, a third investigator (F.B.) had the casting voice.
2.4. Data Items
The extracted data were categorized into the following: study characteristics, NSD assessment method, craniofacial outcome domain, and direction of the reported association. Craniofacial outcome domains included palatal/transverse maxillary morphology, local craniofacial asymmetry, global facial asymmetry, malocclusion or skeletal pattern, basic maxillomandibular dimensions, and nasal volume. These domains were then used to generate a descriptive synthesis, tables, and an evidence map.
2.5. Critical Appraisal
Formal critical appraisal and certainty-of-evidence assessment were not performed, consistent with the purpose of a scoping review, which was to map the available evidence rather than evaluate intervention effects or estimate pooled outcomes.
2.6. Synthesis Methods
Due to the heterogeneity of study designs, NSD assessment methods, imaging protocols, and craniofacial outcome measures, quantitative synthesis was not performed. Results were synthesized descriptively and presented in comparative tables.
5. Limitations
This review has several significant limitations that should be considered when interpreting the results, for example, differences in sample sizes, patient age, inclusion criteria, imaging modalities and the way NSD was described and graded.
First, the number of studies meeting the inclusion criteria was small, and their study designs were significantly heterogeneous. This limits the ability to draw broad generalizations and means that the resulting picture should be considered primarily as a map of research directions rather than a basis for strong causal statements.
Second, the included studies differed in both the way they defined NSD and the type of outcome measures analyzed. The Mladina classification, angular parameters, assessment of posterior curve location, and 3D volumetric analysis do not precisely describe the same measurement construct. At the same time, the endpoints examined covered a very wide spectrum—from palatal depth and facial asymmetry to malocclusion and nasal volume. It is also worth mentioning that there were differences in imaging protocols between included studies. This heterogeneity limits the synthetic interpretation of the results.
Third, the majority of the included data came from observational studies of a cross-sectional or retrospective nature. Such designs allow for the assessment of co-occurrence of features but do not allow for causal inference. Therefore, even significant associations between NSD and selected craniofacial parameters cannot be interpreted as evidence of a direct effect of NSD on facial skeletal development.
Fourth, in the case of Ryu, a working paper based on a translation of the abstract and basic methodological data was used, rather than a complete, native extraction from the published full-text article. Although this material was sufficient to map the direction of the results, the level of detail in this study was less than in the other studies [
23].
Fifth, this scoping review did not conduct a formal assessment of methodological quality or level of evidence. This was consistent with the review’s goal of comprehensively mapping the available literature, rather than hierarchically assessing the strength of evidence. This means that the presented results should be interpreted as a description of the structure and scope of the research field, not as a ranking of the credibility of individual conclusions.
Summing it up, this scoping review should be seen as a map of existing evidence and not as a basis for definitive causal inference.
6. Conclusions
NSD should not currently be interpreted as a uniform marker of global craniofacial morphological abnormalities. The available evidence suggests that NSD assessment methods, including the Mladina classification and other standardized quantitative approaches, may be associated with selected local or transverse features of the nasomaxillary complex, particularly within the palate, nasal floor, maxilla, and adjacent dentoalveolar structures. However, the evidence remains limited, heterogeneous, and inconsistent across outcome domains, especially with regard to global facial asymmetry, basic maxillomandibular dimensions, and malocclusion patterns.
Because the included studies differed substantially in NSD classification or measurement methods, imaging protocols, populations, and craniofacial outcomes, the findings should be interpreted as a map of the available evidence rather than as proof of causality. Current data do not allow for the determination of whether NSD directly contributes to craniofacial development or merely co-occurs with selected morphological patterns. Future studies should combine standardized NSD classifications, particularly the Mladina system, with precise three-dimensional craniofacial assessment in more homogeneous populations. Such an approach may help clarify which specific NSD phenotypes are associated with defined local or transverse craniofacial features and whether these associations have developmental or clinical significance.