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Review
. 2018 Jan 1;9(1):268-274.
doi: 10.1080/19491034.2018.1462635.

Clinical aspects of Emery-Dreifuss muscular dystrophy

Affiliations
Review

Clinical aspects of Emery-Dreifuss muscular dystrophy

Agnieszka Madej-Pilarczyk. Nucleus. .

Abstract

Emery-Dreifuss muscular dystrophy (EDMD), clinically characterized by scapulo-humero-peroneal muscle atrophy and weakness, multi-joint contractures with spine rigidity and cardiomyopathy with conduction defects, is associated with structural/functional defect of genes that encode the proteins of nuclear envelope, including lamin A and several lamin-interacting proteins. This paper presents clinical aspects of EDMD in context to causative genes, genotype-phenotype correlation and its emplacement within phenotypic spectrum of skeletal muscle diseases associated with envelopathies.

Keywords: Emery-Dreifuss muscular dystrophy; cardiomyopathy; emerin; lamin A/C; laminopathy.

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