Microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome

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, WOODS syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome itself.