Browse

Explore conditions, clinical trials, and the organisations running them.

Up to: Syndromic disease · Mitochondrial encephalomyopathy

MELAS syndrome

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.

13 trials tagged with this condition →

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