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Neurol India ; 2006 Jun; 54(2): 197-9
Article in English | IMSEAR | ID: sea-120140

ABSTRACT

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.


Subject(s)
Adolescent , Adult , Humans , Male , Membrane Proteins/deficiency , Muscle, Skeletal/pathology , Muscular Dystrophy, Emery-Dreifuss/diagnosis , Nuclear Proteins , Phenotype , Thymopoietins/deficiency
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