Mitochondrial encephalomyopathy, lactic
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Betty Koo; Laurence E. Becker; Sylvester Chuang; Frank Merante; Brian H. Robinso
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Article
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1993
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John Wiley and Sons
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English
β 870 KB
We reviewed 10 patients (5 males, 5 females) with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes. The age of symptom onset ranged from 3 months to 12 years. All had lactic acidosis, multiple stroke-like events with secondary neurological deficits, radiological changes of