Late-onset multiple acyl-CoA dehydrogenase deficiency mimicking myositis in an elderly patient: a case report

BACKGROUND: Late-onset multiple acyl-CoA dehydrogenase deficiency (MADD) is a rare and treatable inherited lipid storage myopathy. Here, we report an elderly patient with MADD mimicking myositis. CASE PRESENTATION: An 80-year-old woman had progressive weakness in her limbs, exercise intolerance, and...

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Detalles Bibliográficos
Autores principales: Zheng, Yiming, Zhao, Yawen, Zhang, Wei, Wang, Zhaoxia, Yuan, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709274/
https://www.ncbi.nlm.nih.gov/pubmed/33267805
http://dx.doi.org/10.1186/s12883-020-02010-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709274/
https://www.ncbi.nlm.nih.gov/pubmed/33267805
http://dx.doi.org/10.1186/s12883-020-02010-w

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