Mitochondrial cytopathy with common MELAS mutation presenting as multiple system atrophy mimic
نویسندگان
چکیده
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome1 is one of the most frequently inherited mitochondrial disorders. MELAS syndrome is a systemic disease with multiple organ involvement.2 The most common mutation in MELAS is the m.3243A>G mutation in the MT-TL1 gene.2.
منابع مشابه
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