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Up to: Hereditary neurological disease · Monogenic epilepsy
Polyhydramnios, megalencephaly, and symptomatic epilepsy
A syndrome characterized by polyhydramnios, distinctive craniofacial features, infantile-onset epilepsy, hypotonia, macrocephaly, and global developmental delay that has material basis in homozygous mutation in the STRADA gene on chromosome 17q23.3.
This condition has no sub-types.