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PMID: 1635810 Published · ppublish English Journal Article Review

Current status of Duchenne muscular dystrophy.

Pediatric clinics of North America ·Vol. 39 ·No. 4 ·1992-08-00 ·Pages 879-94

Iannaccone ST

Abstract

Duchenne muscular dystrophy is the second most common lethal genetic disorder in humans. With the advent of molecular genetic technology, the definition of this disease has been modified to include an abnormality of dystrophin in muscle--a dystrophinopathy. Accurate genetic counseling is possible using methods of deletion detection and linkage analysis. Treatment of this type of muscular dystrophy may soon mean the routine use of steroids and later include direct injection of an artificial gene for dystrophin.

MeSH Terms
Adult Biopsy Child Humans Male Muscles/pathology Muscular Dystrophies/complications,pathology,therapy
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Iannaccone S T
University of Texas Southwestern Medical School, Dallas.
Article Info
Journal
Pediatric clinics of North America
Abbr.
Pediatr Clin North Am
ISSN
0031-3955
Published
1992-08-00
Pages
879-94
Language
English
Region
United States
NLM ID
0401126
Subset
IM
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