Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the CDKL5 gene.
Comprehensive, easy-to-understand information about this condition
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Mowat-Wilson syndrome
MONDO:0009341
severe neonatal-onset encephalopathy with microcephaly
MONDO:0010397
familial infantile myoclonic epilepsy
MONDO:0011506
neuronal ceroid lipofuscinosis 8 northern epilepsy variant
MONDO:0012391
polyhydramnios, megalencephaly, and symptomatic epilepsy
MONDO:0012611
neonatal-onset encephalopathy with rigidity and seizures
MONDO:0013784