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

Abstract 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 intoleran...

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Hlavní autoři:	Yiming Zheng, Yawen Zhao, Wei Zhang, Zhaoxia Wang, Yun Yuan
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	BMC 2020-12-01
Edice:	BMC Neurology
Témata:	MADD Myositis Lipid storage myopathy Case report
On-line přístup:	https://doi.org/10.1186/s12883-020-02010-w
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