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Road to conception and successful delivery for a facioscapulohumeral muscular dystrophy patient
Facioscapulohumeral muscular dystrophy is a muscular dystrophy affecting all ages, primarily people in the second decade. The disease is initially presented with face, shoulder girdle, and upper arm involvement, followed by lower extremity muscle weakness. Disease progression is usually slow, althou...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891829/ https://www.ncbi.nlm.nih.gov/pubmed/35251661 http://dx.doi.org/10.1177/2050313X221081359 |
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author | Triantafyllidou, Olga Stavridis, Konstantinos Kastora, Stavroula Lila Vlahos, Nikolaos |
author_facet | Triantafyllidou, Olga Stavridis, Konstantinos Kastora, Stavroula Lila Vlahos, Nikolaos |
author_sort | Triantafyllidou, Olga |
collection | PubMed |
description | Facioscapulohumeral muscular dystrophy is a muscular dystrophy affecting all ages, primarily people in the second decade. The disease is initially presented with face, shoulder girdle, and upper arm involvement, followed by lower extremity muscle weakness. Disease progression is usually slow, although about one-fifth of patients will require a wheelchair to accommodate mobility. Women with this muscular dystrophy could rarely have poor birth outcomes, with facioscapulohumeral muscular dystrophy symptom deterioration post-partum. In this study, we present a case of a woman with a genetically confirmed facioscapulohumeral muscular dystrophy 1 who underwent cesarean section with epidural anesthesia with favorable outcomes following the procedure. Eight months post cesarean section, the patient reported no facioscapulohumeral muscular dystrophy symptom deterioration. We reviewed the literature with emphasis on large studies concerning facioscapulohumeral muscular dystrophy and birth outcomes and concluded that the hereby presented approach is important for the comprehensive obstetric care and future risk assessment and management in such patients. |
format | Online Article Text |
id | pubmed-8891829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-88918292022-03-04 Road to conception and successful delivery for a facioscapulohumeral muscular dystrophy patient Triantafyllidou, Olga Stavridis, Konstantinos Kastora, Stavroula Lila Vlahos, Nikolaos SAGE Open Med Case Rep Case Report Facioscapulohumeral muscular dystrophy is a muscular dystrophy affecting all ages, primarily people in the second decade. The disease is initially presented with face, shoulder girdle, and upper arm involvement, followed by lower extremity muscle weakness. Disease progression is usually slow, although about one-fifth of patients will require a wheelchair to accommodate mobility. Women with this muscular dystrophy could rarely have poor birth outcomes, with facioscapulohumeral muscular dystrophy symptom deterioration post-partum. In this study, we present a case of a woman with a genetically confirmed facioscapulohumeral muscular dystrophy 1 who underwent cesarean section with epidural anesthesia with favorable outcomes following the procedure. Eight months post cesarean section, the patient reported no facioscapulohumeral muscular dystrophy symptom deterioration. We reviewed the literature with emphasis on large studies concerning facioscapulohumeral muscular dystrophy and birth outcomes and concluded that the hereby presented approach is important for the comprehensive obstetric care and future risk assessment and management in such patients. SAGE Publications 2022-02-28 /pmc/articles/PMC8891829/ /pubmed/35251661 http://dx.doi.org/10.1177/2050313X221081359 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Report Triantafyllidou, Olga Stavridis, Konstantinos Kastora, Stavroula Lila Vlahos, Nikolaos Road to conception and successful delivery for a facioscapulohumeral muscular dystrophy patient |
title | Road to conception and successful delivery for a facioscapulohumeral muscular dystrophy patient |
title_full | Road to conception and successful delivery for a facioscapulohumeral muscular dystrophy patient |
title_fullStr | Road to conception and successful delivery for a facioscapulohumeral muscular dystrophy patient |
title_full_unstemmed | Road to conception and successful delivery for a facioscapulohumeral muscular dystrophy patient |
title_short | Road to conception and successful delivery for a facioscapulohumeral muscular dystrophy patient |
title_sort | road to conception and successful delivery for a facioscapulohumeral muscular dystrophy patient |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891829/ https://www.ncbi.nlm.nih.gov/pubmed/35251661 http://dx.doi.org/10.1177/2050313X221081359 |
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