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Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome
rareCapra-DeMarco syndrome is characterized by sagittal craniosynostosis, hydrocephalus, Chiari I malformation and radioulnar synostosis. Other clinical findings include blepharophimosis, small low-set ears, hypoplastic philtrum, kidney malformation, and hypogenitalism.
- Identifiers
- MONDO:0015751 Orphanet:171839
- Part of
- Syndromic craniosynostosis
- Also known as
- Berant syndrome · Capra-DeMarco syndrome · familial scaphocephaly-radioulnar synostosis syndrome
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