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Neurol India ; 2006 Jun; 54(2): 197-9
Artigo em Inglês | IMSEAR | ID: sea-120140

RESUMO

Emery-Dreifuss muscular dystrophy (EDMD) is a rare and genetically heterogeneous disorder. We report two patients with emerin deficient X-linked EDMD and two probable patients with EDMD with typical early contractures, progressive muscle weakness and cardiac involvement. Family history was noted in one case. Muscle biopsy revealed features of dystrophy in all.


Assuntos
Adolescente , Adulto , Humanos , Masculino , Proteínas de Membrana/deficiência , Músculo Esquelético/patologia , Distrofia Muscular de Emery-Dreifuss/diagnóstico , Proteínas Nucleares , Fenótipo , Timopoietinas/deficiência
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