Article
Neuroanatomy in Rett syndrome
1 Feb 1997
Abstract excerpt
Rett syndrome (RS), a neurodevelopmental disorder of unknown etiology occurring almost exclusively in females, is characterized by autistic-like behavior, motor dysfunction, loss of language skills, dementia, and microcephaly. This study is a follow-up and extension of a previously reported neuroimaging study of patients with RS. We replicated previously reported findings with a larger patient population, and the...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
