Limb-girdle muscular dystrophy type 2B misdiagnosed as polymyositis at the early stage: Case report and literature review

RATIONALE: Dysferlin myopathy is an autosomal recessive hereditary muscular dystrophy due to deficiency of dysferlin caused by alteration of the DYSF gene; Limb-girdle muscular dystrophy type 2B (LGMD2B) is the most common in Its clinical phenotypes. However, LGMD2B is rarely seen in clinical cases...

Descripción completa

Detalles Bibliográficos
Autores principales: Xu, Chuan, Chen, Jiajun, Zhang, Yingyu, Li, Jia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6392577/
https://www.ncbi.nlm.nih.gov/pubmed/29794729
http://dx.doi.org/10.1097/MD.0000000000010539

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6392577/
https://www.ncbi.nlm.nih.gov/pubmed/29794729
http://dx.doi.org/10.1097/MD.0000000000010539

Ejemplares similares