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Up to: Hereditary neurological disease · Monogenic epilepsy · Neonatal epilepsy syndrome · Mendelian encephalopathy
Severe neonatal-onset encephalopathy with microcephaly
An X-linked recessive condition caused by mutation(s) in the MECP2 gene, encoding methyl-CpG-binding protein 2. It is characterized by severe neonatal encephalopathy.
This condition has no sub-types.