| Summary points: | A 34-year-old Saudi woman presents with clinical symptoms suggestive of mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS). At age 24, she started to have generalised tonic-clonic seizures; at age 27, she lost her vision and hearing; and at age 32, she developed right-sided weakness. Medical history, brain imaging, and histochemical analysis are described. The authors discuss the case of a patient with typical clinical features of MELAS, but without an obvious genetic cause. |
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A Patient with Typical Clinical Features of Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS) but Without an Obvious Genetic Cause: A Case Report
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