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Atypical onset in a series of 122 cases with FacioScapuloHumeral Muscular Dystrophy
INTRODUCTION: FacioScapuloHumeral Muscular Dystrophy (FSHD), a disease linked to a heterozygous D4Z4 deletion on chromosome 4q35, typically starts with shoulder-girdle and facial muscle involvement. Atypical presentations have occasionally been reported, but their frequency has still not been define...
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| Главные авторы: | , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Elsevier
2012
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3314982/ https://ncbi.nlm.nih.gov/pubmed/22079131 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.clineuro.2011.10.022 |
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