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.

Also known as: encephalopathy, neonatal severe, X-linked recessive, severe congenital encephalopathy due to MECP2 mutation, severe neonatal encephalopathy due to MECP2 mutations, encephalopathy, neonatal severe, due to MECP2 mutations

7 clinical trials for this condition and its sub-types, 0 tagged with Severe neonatal-onset encephalopathy with microcephaly itself.