MELAS syndrome (Q2666433)

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one of the family of mitochondrial cytopathies, which also include MERRF, and Leber's hereditary optic neuropathy
  • mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
  • MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES
  • Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes
  • Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes
  • MELAS
  • Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke
  • MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS
  • Melas Syndrome
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Language Label Description Also known as
English
MELAS syndrome
one of the family of mitochondrial cytopathies, which also include MERRF, and Leber's hereditary optic neuropathy
  • mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
  • MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES
  • Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes
  • Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes
  • MELAS
  • Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke
  • MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS
  • Melas Syndrome

Statements

Двусторонняя кальцификация базальных ганглев, легкая атрофия мозжечка, ишемические изменения, повышение лактата. Abu-Amero et al., 2009[1] (Russian)
MELAS syndrome
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