Jan 25, 2024 · MELAS is characterized by progressive deterioration of the nervous system that leads to neurological impairment and dementia in adolescence or ...
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syndrome is a rare disorder that begins in childhood, usually between two and fifteen years of age, and mostly affects the nervous system and muscles.
MELAS syndrome is a mitochondrial disease that's caused by genetic mutations, or changes. It's passed down by mothers even though it can affect anyone.
Jan 21, 2020 · Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke (MELAS) syndrome is a progressive neurodegenerative disorder.
MELAS syndrome
Disease
Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes is one of the family of mitochondrial diseases, which also include MIDD, MERRF syndrome, and Leber's hereditary optic neuropathy. It was first characterized under this name in... Wikipedia
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) is an extremely rare genetic condition that begins in childhood. The disorder ...
Dec 1, 2013 · Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) is a condition that affects many of the body's systems, ...
Mitochondrial Encephalomyopathy With Lactic Acidosis and Stroke ...
www.ncbi.nlm.nih.gov › PMC5625994
Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome is a rare inherited disorder that results in waxing and waning ...
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