Clinical Genetics · 1993 · 11 citations · 17 references
DentistryCraniofacial BiologyCraniofacial DevelopmentCraniofacial GeneticsHuman GeneticsCephalometric AnalysisCephalometric ImagingCephalometric RadiographyCongenital Craniofacial AnomaliesCraniofacial AnomaliesThree-dimensional Cephalometric AnalysisAnthropometric Facial MeasurementCephalometric Morphometric AnalysisCranial AnthropometryCraniofacial MeasurementsCraniofacial Morphometric AnalysisCraniofacial MorphometricsIntercanthal DistanceLinear Discriminant Analysis
da‐Silva EO, Batista JEM, Medeiros MAB, Fonteles SMS. Craniofacial anthropometric studies in Waardenburg syndrome type I. Clin Genet 1993: 44: 20–25. © Munksgaard, 1993 A set of 15 surface measurements taken directly from the craniofacial region were determined in 51 patients with Waardenburg syndrome type I (WSI). A roentgencephamometric analysis including 20 linear dimensions was also performed by the use of cephalograms of 28 patients. Pairs between patients and controls of the same sex and age were established for comparison. The head circumference, clivus length and facial depth were smaller in affected individuals. The patients also had narrow nose, marked hypoplasia of the nasal bone, short philtrum, and short and retropositioned maxilla. A discriminant analysis revealed that the inner intercanthal distance, philtrum length, lower facial height and nasal bone length were excellent discriminating parameters of WSI.
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An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome
Clinton T. Baldwin, Christopher F. Hoth, Jean Amos et al. · Nature · 1992 · 459 citations
Craniofacial morphology in Turner syndrome.
B L Jensen · PubMed · 1985 · 49 citations
Medicine, Craniofacial Biology, Craniofacial Development +16