Literature DB >> 3319295

X-linked muscular dystrophy with early contractures and cardiomyopathy (Emery-Dreifuss type).

A E Emery1.   

Abstract

The original Virginia family with X-linked muscular dystrophy with early contractures and cardiomyopathy (Emery-Dreifuss type) has been reinvestigated 25 years later. The findings confirm that a cardiomyopathy, presenting most often as atrioventricular block, is a significant feature of the disease, which is characterized by the triad of: 1) slowly progressive muscle wasting and weakness with a humero-peroneal distribution in the early stages; 2) early contractures of the elbows, Achilles tendons, and post-cervical muscles; and 3) a cardiomyopathy usually presenting as heart block (some female carriers may also develop heart block). Other reported families with X-linked Emery-Dreifuss muscular dystrophy as well as a rare autosomal variant are reviewed, and differentiation from scapulo-peroneal muscular dystrophy and the rigid spine syndrome is discussed.

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Year:  1987        PMID: 3319295     DOI: 10.1111/j.1399-0004.1987.tb03302.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  18 in total

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Review 7.  Congenital and idiopathic scoliosis: clinical and genetic aspects.

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Review 8.  Genetic abnormalities responsible for dilated cardiomyopathy.

Authors:  J A Towbin; N E Bowles
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9.  Mapping of the Emery-Dreifuss gene through reconstruction of crossover points in two Italian pedigrees.

Authors:  G Romeo; L Roncuzzi; S Sangiorgi; M Giacanelli; M Liguori; D Tessarolo; M Rocchi
Journal:  Hum Genet       Date:  1988-09       Impact factor: 4.132

10.  Creatine supplementation in health and disease. Effects of chronic creatine ingestion in vivo: down-regulation of the expression of creatine transporter isoforms in skeletal muscle.

Authors:  M L Guerrero-Ontiveros; T Wallimann
Journal:  Mol Cell Biochem       Date:  1998-07       Impact factor: 3.396

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