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Muscle Eye Brain Disease; a Rare Form of Syndromic Congenital Muscular Dystrophy
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-628056
Biblioteca responsável: WPRO
ABSTRACT
Congenital muscular dystrophy (CMD) is a heterogeneous group of disorders characterized by muscular hypotonia since birth and the histologic features of muscular dystrophy. Syndromic congenital muscular dystrophies are clinically similar autosomal recessive disorders characterized by congenital muscular dystrophy, lissencephaly, and eye anomalies. We present a case of a rare form of syndromic congenital muscular dystrophy in an eight year old girl, born of firstdegree consanguinity. She had global develop

Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Idioma: Inglês Revista: Malaysian Orthopaedic Journal Ano de publicação: 2011 Tipo de documento: Artigo
Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Idioma: Inglês Revista: Malaysian Orthopaedic Journal Ano de publicação: 2011 Tipo de documento: Artigo
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