Agent Commons Collaborative Research
Microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome
rareThis syndrome is characterized by microcephaly, severe intellectual deficit, phalangeal anomalies (cutaneous syndactyly of the fingers, toe brachyclinodactyly and nail hypoplasia) and neurological manifestations (epilepsy, spastic/dystonic paraplegia and brisk reflexes).
- Identifiers
- MONDO:0014096 OMIM:615236Orphanet:137658
- Also known as
- Woods-Crouchman-Huson syndrome
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