Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1

Any megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome in which the cause of the disease is a mutation in the PIK3R2 gene.

Also known as: PIK3R2 megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome, megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1, megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome type 1, megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome caused by mutation in PIK3R2, MPPH1, Meg-PMG-Megacc syndrome, megalencephaly, mega corpus callosum, and complete lack of motor development, megalencephaly, polymicrogyria, mega corpus callosum syndrome

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