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Late-Onset Dystrophinopathy
Dystrophinopathy is a spectrum of muscular dystrophies resulting from absolute to relative deficiency of dystrophin - a protein essential for muscle fiber integrity. This includes a severe form called Duchenne muscular dystrophy, a mild form called Becker muscular dystrophy, and intermediate muscula...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8765568/ https://www.ncbi.nlm.nih.gov/pubmed/35070564 http://dx.doi.org/10.7759/cureus.20531 |
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author | Singh, Ranjan K |
author_facet | Singh, Ranjan K |
author_sort | Singh, Ranjan K |
collection | PubMed |
description | Dystrophinopathy is a spectrum of muscular dystrophies resulting from absolute to relative deficiency of dystrophin - a protein essential for muscle fiber integrity. This includes a severe form called Duchenne muscular dystrophy, a mild form called Becker muscular dystrophy, and intermediate muscular dystrophy. Becker muscular dystrophy relates to late-onset and slow progression muscle dystrophy caused by deletions or duplications in the dystrophin gene. Individuals with this type of tardive slow progression have a life expectancy of 60 years. A patient in his late 40s presented this disease with duplication of exon 2 in the dystrophin gene. |
format | Online Article Text |
id | pubmed-8765568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-87655682022-01-21 Late-Onset Dystrophinopathy Singh, Ranjan K Cureus Cardiology Dystrophinopathy is a spectrum of muscular dystrophies resulting from absolute to relative deficiency of dystrophin - a protein essential for muscle fiber integrity. This includes a severe form called Duchenne muscular dystrophy, a mild form called Becker muscular dystrophy, and intermediate muscular dystrophy. Becker muscular dystrophy relates to late-onset and slow progression muscle dystrophy caused by deletions or duplications in the dystrophin gene. Individuals with this type of tardive slow progression have a life expectancy of 60 years. A patient in his late 40s presented this disease with duplication of exon 2 in the dystrophin gene. Cureus 2021-12-20 /pmc/articles/PMC8765568/ /pubmed/35070564 http://dx.doi.org/10.7759/cureus.20531 Text en Copyright © 2021, Singh et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Cardiology Singh, Ranjan K Late-Onset Dystrophinopathy |
title | Late-Onset Dystrophinopathy |
title_full | Late-Onset Dystrophinopathy |
title_fullStr | Late-Onset Dystrophinopathy |
title_full_unstemmed | Late-Onset Dystrophinopathy |
title_short | Late-Onset Dystrophinopathy |
title_sort | late-onset dystrophinopathy |
topic | Cardiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8765568/ https://www.ncbi.nlm.nih.gov/pubmed/35070564 http://dx.doi.org/10.7759/cureus.20531 |
work_keys_str_mv | AT singhranjank lateonsetdystrophinopathy |