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Up to: Lennox-Gastaut syndrome · Undetermined early-onset epileptic encephalopathy · Neonatal-onset developmental and epileptic encephalopathy · DNM1-encephalopathy and neurodevelopmental disorder
Developmental and epileptic encephalopathy, 31A
Any developmental and epileptic encephalopathy in which the cause of the disease is a heterozygous mutation in the DNM1 gene.
This condition has no sub-types.