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Up to: Genetic developmental and epileptic encephalopathy · Infantile spasms · Atypical Rett syndrome · Monogenic epilepsy · CDKL5 disorder
Developmental and epileptic encephalopathy, 2
Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the CDKL5 gene.
This condition has no sub-types.