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Phenotypic contrasts of Duchenne Muscular Dystrophy in women: Two case reports

We discussed two cases of symptomatic female carriers to Duchenne Muscular Dystrophy. The first case is a 20 year-old girl with classical phenotypic manifestation of the disease, similar to the condition in boys. The case 2 is a 62 year-old woman with progressive muscular weakness. The disease is mu...

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Autores principales: Nozoe, Karen T., Akamine, Ricardo T., Mazzotti, Diego R., Polesel, Daniel N., Grossklauss, Luís F., Tufik, Sergio, Andersen, Monica L., Moreira, Gustavo A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5241604/
https://www.ncbi.nlm.nih.gov/pubmed/28123647
http://dx.doi.org/10.1016/j.slsci.2016.07.004
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author Nozoe, Karen T.
Akamine, Ricardo T.
Mazzotti, Diego R.
Polesel, Daniel N.
Grossklauss, Luís F.
Tufik, Sergio
Andersen, Monica L.
Moreira, Gustavo A.
author_facet Nozoe, Karen T.
Akamine, Ricardo T.
Mazzotti, Diego R.
Polesel, Daniel N.
Grossklauss, Luís F.
Tufik, Sergio
Andersen, Monica L.
Moreira, Gustavo A.
author_sort Nozoe, Karen T.
collection PubMed
description We discussed two cases of symptomatic female carriers to Duchenne Muscular Dystrophy. The first case is a 20 year-old girl with classical phenotypic manifestation of the disease, similar to the condition in boys. The case 2 is a 62 year-old woman with progressive muscular weakness. The disease is much less common in woman than men so both cases described here are considered rare forms of the disease, with several clinical implications. In both cases, a progressive muscle weakness, impairment in walking and sleeping was observed, in addition to obstructive sleep apnea syndrome and alveolar hypoventilation, that required noninvasive ventilatory support.
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spelling pubmed-52416042017-01-25 Phenotypic contrasts of Duchenne Muscular Dystrophy in women: Two case reports Nozoe, Karen T. Akamine, Ricardo T. Mazzotti, Diego R. Polesel, Daniel N. Grossklauss, Luís F. Tufik, Sergio Andersen, Monica L. Moreira, Gustavo A. Sleep Sci Case Report We discussed two cases of symptomatic female carriers to Duchenne Muscular Dystrophy. The first case is a 20 year-old girl with classical phenotypic manifestation of the disease, similar to the condition in boys. The case 2 is a 62 year-old woman with progressive muscular weakness. The disease is much less common in woman than men so both cases described here are considered rare forms of the disease, with several clinical implications. In both cases, a progressive muscle weakness, impairment in walking and sleeping was observed, in addition to obstructive sleep apnea syndrome and alveolar hypoventilation, that required noninvasive ventilatory support. Elsevier 2016 2016-08-18 /pmc/articles/PMC5241604/ /pubmed/28123647 http://dx.doi.org/10.1016/j.slsci.2016.07.004 Text en © 2016 Brazilian Association of Sleep. Production and Hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Nozoe, Karen T.
Akamine, Ricardo T.
Mazzotti, Diego R.
Polesel, Daniel N.
Grossklauss, Luís F.
Tufik, Sergio
Andersen, Monica L.
Moreira, Gustavo A.
Phenotypic contrasts of Duchenne Muscular Dystrophy in women: Two case reports
title Phenotypic contrasts of Duchenne Muscular Dystrophy in women: Two case reports
title_full Phenotypic contrasts of Duchenne Muscular Dystrophy in women: Two case reports
title_fullStr Phenotypic contrasts of Duchenne Muscular Dystrophy in women: Two case reports
title_full_unstemmed Phenotypic contrasts of Duchenne Muscular Dystrophy in women: Two case reports
title_short Phenotypic contrasts of Duchenne Muscular Dystrophy in women: Two case reports
title_sort phenotypic contrasts of duchenne muscular dystrophy in women: two case reports
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5241604/
https://www.ncbi.nlm.nih.gov/pubmed/28123647
http://dx.doi.org/10.1016/j.slsci.2016.07.004
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