Literature DB >> 3729752

Autosomal dominant humeroperoneal myopathy.

J M Gilchrist, R T Leshner.   

Abstract

Emery-Dreifuss muscular dystrophy is a syndrome with five salient features: early and unusual contractures; humeroperoneal muscle wasting; the slow progression of weakness, beginning in childhood; cardiac conduction defects; and X-linked inheritance. We present two cases and detail other reports with a similar constellation of findings with apparent autosomal dominant inheritance. We postulate separate genetic disorders with similar phenotypic expression.

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Year:  1986        PMID: 3729752     DOI: 10.1001/archneur.1986.00520070088026

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  2 in total

1.  Emery-Dreifuss muscular dystrophy in the evaluation of decreased spinal mobility and joint contractures.

Authors:  Kamil Goncu; Rengin Guzel; Fusun Guler-Uysal
Journal:  Clin Rheumatol       Date:  2003-10-21       Impact factor: 2.980

2.  The heart in limb girdle muscular dystrophy.

Authors:  A J van der Kooi; W G de Voogt; P G Barth; H F Busch; F G Jennekens; P J Jongen; M de Visser
Journal:  Heart       Date:  1998-01       Impact factor: 5.994

  2 in total

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