Clinical insights into mitochondrial retinopathy: A case report on m.3243A>G mutation and macular dystrophy
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Mitochondrial disorders, particularly those associated with the m.3243A>G mutation in the MT-TL1 gene, can manifest with diverse systemic and ocular features, including mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) a... ...
