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PMID: 1355417 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Variable dystrophin expression in different muscles of a Duchenne muscular dystrophy carrier.

Clinical genetics ·Vol. 42 ·No. 1 ·1992-07-00 ·Pages 35-8

Muntoni F, Mateddu A, Marrosu MG, Cau M, Congiu R, Melis MA, Cao A, Cianchetti C

Abstract

The majority of Duchenne muscular dystrophy (DMD) female carriers show dystrophin immunostaining abnormalities, although a significant proportion of clinically non-manifesting carriers are normal following this analysis. We had the opportunity to study dystrophin immunostaining in two different muscles, the vastus lateralis and the rectus abdominis of a possible DMD carrier. While the vastus showed normal dystrophin immunostaining, pathological staining was detected in her rectus abdominis. These findings seem to indicate that dystrophin expression can vary in different muscle groups of a DMD carrier. The implications of these findings in DMD carrier detection and possible dystrophin function are discussed.

MeSH Terms
Adult Dystrophin/analysis,genetics Female Heterozygote Humans Immunohistochemistry Middle Aged Muscles/metabolism Muscular Dystrophies/genetics,metabolism Polymerase Chain Reaction Polymorphism, Restriction Fragment Length
Chemicals
Dystrophin
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Muntoni F
Instituto di Neuropsichiatria Infantile, Cagliari, Italy.
Mateddu A
Marrosu M G
Cau M
Congiu R
Melis M A
Cao A
Cianchetti C
Article Info
Journal
Clinical genetics
Abbr.
Clin Genet
ISSN
0009-9163
Published
1992-07-00
Pages
35-8
Language
English
Region
Denmark
NLM ID
0253664
Subset
IM
Grants
Telethon · 15 · Italy
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