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Lipid-storage myopathy with glycogen storage disease gene mutations mimicking polymyositis: a case report and review of the literature

A 26-year-old Asian woman with persistent muscle weakness was diagnosed with polymyositis based on biopsy findings at another hospital 11 years ago. However, her symptoms fluctuated repeatedly under treatment with prednisone and immunosuppressive agents, and worsened 2 months prior to the current pr...

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Detalles Bibliográficos
Autores principales: Pan, Xiaoli, Yuan, Yuan, Wu, Bangcui, Zheng, Wendan, Tian, Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943314/
https://www.ncbi.nlm.nih.gov/pubmed/35296144
http://dx.doi.org/10.1177/03000605221084873