Developmental and epileptic encephalopathy, 32

MONDO:0014607

Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the KCNA2 gene.

Also known as: DEE32, EIEE32, KCNA2 early infantile epileptic encephalopathy, developmental and epileptic encephalopathy 32, early infantile epileptic encephalopathy caused by mutation in KCNA2, epileptic encephalopathy, early infantile, 32, epileptic encephalopathy, early infantile, type 32

17 clinical trials for this condition and its sub-types, 0 tagged with Developmental and epileptic encephalopathy, 32 itself.

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↑ Undetermined early-onset epileptic encephalopathy (6) ↑ Neonatal-onset developmental and epileptic encephalopathy (5)

Including sub-types (17) Tagged with Developmental and epileptic encephalopathy, 32 (0)

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