People with MELAS syndrome have an accumulation of lactic acid in the blood (lactic acidosis), that can lead to vomiting, abdominal pain, fatigue, muscle weakness and difficulty breathing. This accumulation of lactic acid has also been noted in the spinal fluid and in the brain.
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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 25, 2024 · MELAS syndrome is a rare mitochondrial disease primarily affecting the nervous system and muscles. Diagnosing MELAS can be challenging due to ...
MELAS syndrome
Disease
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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-like episodes (MELAS) syndrome is a rare inherited disorder that results in waxing and waning ...
Jan 21, 2020 · Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke (MELAS) syndrome is a progressive neurodegenerative disorder.
Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) is a progressive multisystem disorder that primarily affects the nervous ...
Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is one of the family of mitochondrial diseases, which also include MIDD ...
A rare neurometabolic genetic disorder which is progressive and multisystemic due to mitochondrial dysfunction and that is characterized by encephalomyopathy, ...
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