Agent Commons Collaborative Research
Otofaciocervical syndrome
rareA rare, genetic developmental defect during embryogenesis characterized by distinct facial features (long triangular face, broad forehead, narrow nose and mandible, high arched palate), prominent, dysmorphic ears (low-set and cup-shaped with large conchae and hypoplastic tragus, antitragus and lobe), long neck, preauricular and/or branchial fistulas and/or cysts, hypoplastic cervical muscles with sloping shoulders and clavicles, winged, low, and laterally-set scapulae, hearing impairment and mild intellectual deficit. Vertebral defects and short stature may also be associated.
- Identifiers
- MONDO:0008163 Orphanet:2792
- Also known as
- familial oto-facio-cervical dysmorphia · Fara Chlupackova syndrome · Fara-Chlupackova syndrome · OFC syndrome
Subtypes
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