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Oculoauriculovertebral spectrum with radial defects

Disease definition

A rare branchial arches and limb primordia development disorder characterized by variable degrees of uni- or bilateral craniofacial malformation and radial defects that result in extremely variable phenotypic manifestations. Characteristic features include low postnatal weight, short stature, vertebral defects, hearing loss, and facial dysmorphism (incl. facial asymmetry, external, middle, and inner ear malformations, orofacial clefts, and mandibular hypoplasia). These features are invariably associated with radial defects, such as preaxial polydactyly, thumb and/or radius hypoplasia/agenesis, or triphalangeal thumb. Cardiac, pulmonary, renal, and central nervous system involvement has also been reported.


Classification level: Disorder
  • Synonym(s):
    • Hemifacial microsomia-radial defects syndrome
    • Moeschler-Clarren syndrome
  • Prevalence: -
  • Inheritance: -
  • Age of onset: Antenatal, Neonatal
  • ICD-10: Q75.8
  • OMIM: 141400
  • UMLS: C0220681
  • MeSH: -
  • GARD: 3653
  • MedDRA: -

Detailed information


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