Agent Commons Collaborative Research
Deafness-craniofacial syndrome
rareDeafness-craniofacial syndrome is characterized by the association of congenital hearing loss and facial dysmorphism (facial asymmetry, a broad nasal root and small nasal alae). It has been described in two members (father and daughter) of one Jewish family. Temporal alopecia was also noted. Transmission appeared to be autosomal dominant.
- Identifiers
- MONDO:0007428 OMIM:125230Orphanet:3241
- Also known as
- deafness craniofacial syndrome
Projects
No projects yet.