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The Canadian experience with long term deflazacort treatment in Duchenne muscular dystrophy
Deflazacort is the most commonly prescribed corticosteroid for the treatment of Duchenne muscular dystrophy in Canada. We review the long term experience with deflazacort treatment at two centers in Canada; Montreal and Toronto. Deflazacort has benefitted both cohorts by prolonged ambulation, preser...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pacini Editore SpA
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3440807/ https://www.ncbi.nlm.nih.gov/pubmed/22655512 |
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author | McADAM, LAURA C. MAYO, AMANDA L. ALMAN, BENJAMIN A. BIGGAR, W. DOUGLAS |
author_facet | McADAM, LAURA C. MAYO, AMANDA L. ALMAN, BENJAMIN A. BIGGAR, W. DOUGLAS |
author_sort | McADAM, LAURA C. |
collection | PubMed |
description | Deflazacort is the most commonly prescribed corticosteroid for the treatment of Duchenne muscular dystrophy in Canada. We review the long term experience with deflazacort treatment at two centers in Canada; Montreal and Toronto. Deflazacort has benefitted both cohorts by prolonged ambulation, preserved cardiac and respiratory function, less scoliosis and improved survival. Common side effects in both cohorts include weight gain, decreased height and cataract formation. The Canadian experience supports the use of deflazacort in treating boys with Duchenne muscular dystrophy. |
format | Online Article Text |
id | pubmed-3440807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Pacini Editore SpA |
record_format | MEDLINE/PubMed |
spelling | pubmed-34408072012-10-12 The Canadian experience with long term deflazacort treatment in Duchenne muscular dystrophy McADAM, LAURA C. MAYO, AMANDA L. ALMAN, BENJAMIN A. BIGGAR, W. DOUGLAS Acta Myol Original Articles Deflazacort is the most commonly prescribed corticosteroid for the treatment of Duchenne muscular dystrophy in Canada. We review the long term experience with deflazacort treatment at two centers in Canada; Montreal and Toronto. Deflazacort has benefitted both cohorts by prolonged ambulation, preserved cardiac and respiratory function, less scoliosis and improved survival. Common side effects in both cohorts include weight gain, decreased height and cataract formation. The Canadian experience supports the use of deflazacort in treating boys with Duchenne muscular dystrophy. Pacini Editore SpA 2012-05 /pmc/articles/PMC3440807/ /pubmed/22655512 Text en The journal and the individual contributions contained in it are protected by the copyright of Gaetano Conte Academy, Naples, Italy http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives License, which permits for noncommercial use, distribution, and reproduction in any digital medium, provided the original work is properly cited and is not altered in any way. For details, please refer to http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Articles McADAM, LAURA C. MAYO, AMANDA L. ALMAN, BENJAMIN A. BIGGAR, W. DOUGLAS The Canadian experience with long term deflazacort treatment in Duchenne muscular dystrophy |
title | The Canadian experience with long term deflazacort treatment in Duchenne muscular dystrophy |
title_full | The Canadian experience with long term deflazacort treatment in Duchenne muscular dystrophy |
title_fullStr | The Canadian experience with long term deflazacort treatment in Duchenne muscular dystrophy |
title_full_unstemmed | The Canadian experience with long term deflazacort treatment in Duchenne muscular dystrophy |
title_short | The Canadian experience with long term deflazacort treatment in Duchenne muscular dystrophy |
title_sort | canadian experience with long term deflazacort treatment in duchenne muscular dystrophy |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3440807/ https://www.ncbi.nlm.nih.gov/pubmed/22655512 |
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