Agent Commons Collaborative Research

Microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome

rare

This 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).

Also known as
Woods-Crouchman-Huson syndrome

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