Literature DB >> 6737006

Severe muscular dystrophy in girls.

D Gardner-Medwin, H M Johnston.   

Abstract

Twelve girls and 2 boys with severe but not congenital muscular dystrophy were found in a national survey. An autosomal recessive gene is likely to account for most if not all of these cases. The condition differs slightly from X-linked Duchenne muscular dystrophy in showing prominent early toe-walking, a milder course, relatively more weakness of the deltoid muscles, normal intelligence, a normal ECG and a more focal pattern of muscle pathology.

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Year:  1984        PMID: 6737006     DOI: 10.1016/0022-510x(84)90058-3

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  5 in total

1.  Brother/sister pairs affected with early-onset, progressive muscular dystrophy: molecular studies reveal etiologic heterogeneity.

Authors:  U Francke; B T Darras; J H Hersh; B O Berg; R G Miller
Journal:  Am J Hum Genet       Date:  1989-07       Impact factor: 11.025

2.  Dystrophin analysis in the diagnosis of muscular dystrophy.

Authors:  A M Norman; H E Hughes; D Gardner-Medwin; L V Nicholson
Journal:  Arch Dis Child       Date:  1989-10       Impact factor: 3.791

3.  Cytogenetic analysis and muscle differentiation in a girl with severe muscular dystrophy.

Authors:  G Meola; E Scarpini; M Velicogna; G Scarlato; L Larizza; A F Conti
Journal:  J Neurol       Date:  1986-06       Impact factor: 4.849

4.  Duchenne muscular dystrophy in one of monozygotic twin girls.

Authors:  J Burn; S Povey; Y Boyd; E A Munro; L West; K Harper; D Thomas
Journal:  J Med Genet       Date:  1986-12       Impact factor: 6.318

Review 5.  The golden retriever model of Duchenne muscular dystrophy.

Authors:  Joe N Kornegay
Journal:  Skelet Muscle       Date:  2017-05-19       Impact factor: 4.912

  5 in total

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