Literature DB >> 6613528

Death in childhood due to facio-scapulo-humeral dystrophy.

J McGarry, B Garg, S Silbert.   

Abstract

Two siblings with facio-scapulo-humeral dystrophy (FSH) had muscle biopsy with light microscopy and histochemistry performed. Rapid disease progression resulted in the death of one child at age 5 years. Such an outcome has not been previously reported.

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Mesh：

Year:  1983        PMID： 6613528     DOI： 10.1111/j.1600-0404.1983.tb04817.x

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN： 0001-6314            Impact factor:   3.209


  3 in total

1.  Hearing loss in facioscapulohumeral dystrophy.

Authors:  T Voit; A Lamprecht; H G Lenard; H H Goebel
Journal:  Eur J Pediatr       Date:  1986-09       Impact factor: 3.183

2.  De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1).

Authors:  P E Jardine; M C Koch; P W Lunt; J Maynard; K D Bathke; P S Harper; M Upadhyaya
Journal:  Arch Dis Child       Date:  1994-09       Impact factor: 3.791

3.  Genetic counselling in facioscapulohumeral muscular dystrophy.

Authors:  P W Lunt; P S Harper
Journal:  J Med Genet       Date:  1991-10       Impact factor: 6.318
  3 in total

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