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Kousseff syndrome
rareA syndrome characterized by the association of conotruncal heart defects, myelomeningocele and craniofacial dysmorphism similar to that seen in monosomy 22q11.
- Identifiers
- MONDO:0016522 Orphanet:2351
- Part of
- Syndromic disease
- Also known as
- sacral meningocele conotruncal heart defects · sacral meningocele, conotruncal heart defects, and minor anomalies of head and neck · sacral meningocele-conotruncal heart defects syndrome
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