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MELAS syndrome

MONDO:0010789

MELAS (Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke) syndrome is a rare progressive multisystemic disorder characterized by encephalomyopathy, lactic acidosis, and stroke-like episodes. Other features include endocrinopathy, heart disease, diabetes, hearing loss, and neurological and psychiatric manifestations.

Also known as: MELAS syndrome, mitochondrial encephalomyopathy, lactic acidosis and stroke, mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes, mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes, mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes, MELAS, mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes

86 clinical trials for this condition and its sub-types.

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Sub-types

MELAS syndrome caused by mutation in MTTL1 (1) MELAS syndrome caused by mutation in MTND1 (0) MELAS syndrome caused by mutation in MTND5 (0) MELAS syndrome caused by mutation in MTND6 (0) MELAS syndrome caused by mutation in MTTC (0) MELAS syndrome caused by mutation in MTTH (0) MELAS syndrome caused by mutation in MTTK (0) MELAS syndrome caused by mutation in MTTQ (0) MELAS syndrome caused by mutation in MTTS1 (0) MELAS syndrome caused by mutation in MTTS2 (0)

Broader categories

Disease (618) Metabolic disease (215) Musculoskeletal system disorder (196) Hereditary disease (172) Inborn mitochondrial metabolism disorder (57) Muscle tissue disorder (53) Inborn errors of metabolism (42) Mitochondrial disease (39) Syndromic disease (24) Inborn mitochondrial myopathy (15)
Trials to join now! 42 Not yet recruiting 12 Not yet finished but already full! 14 Completed 16 Terminated 2
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