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Progressive Encephalopathy in Boys with Symptoms of Rett Syndrome and MECP2 Mutations

Four young boys with neonatal onset of encephalopathy, a progressive course, and MECP2 mutations are reported from the University of Alabama, Birmingham, AL Symptoms suggestive of Rett syndrome included failure to thrive, respiratory insufficiency, microcephaly, hypotonia, movement disorder, with my...

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Hovedforfatter: J Gordon Millichap
Format: Artigo
Sprog:Inglês
Udgivet: Pediatric Neurology Briefs Publishers 2006-08-01
Serier:Pediatric Neurology Briefs
Fag:
progressive encephalopathy
rett syndrome
mecp2 mutations
Online adgang:https://www.pediatricneurologybriefs.com/articles/1121
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