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Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis

MONDO:0014679

Also known as: polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis, PMGYCHA

0 clinical trials for this condition and its sub-types.

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Broader categories

Disease (680) Nervous system disorder (231) Hereditary disease (176) Human disease (14) Hereditary neurological disease (6) Disease of genetic or genomic mechanism (2) Congenital nervous system disorder (1) Polymicrogyria (1) Bilateral perisylvian polymicrogyria (0) Bilateral polymicrogyria (0)

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