Clinical characteristics of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes

HIGHLIGHTS

  • who: Hueng-Chuen Fan et al. from the Department of Pediatrics, Tungs' Taichung Metroharbor Hospital, Wuchi, Taichung, TaiwanDepartment of Life Sciences, Agricultural Biotechnology Center, National Chung Hsing University have published the article: Clinical Characteristics of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes, in the Journal: Life 2021, 11, 1111. of /2021/
  • what: MELAS syndrome is a maternally inherited mitochondrial disease with broad manifestations, including encephalomyopathies such as dementia, epilepsy, and myopathy, lactic acidemia, and stroke-like episodes.

SUMMARY

    The functions of mitochondria include the biosynthesis of amino_acids, fatty_acids, vitamin cofactors . . .

     

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