Mitochondrial Encephalomyopathy

Mitochondrial Encephalomyopathy is a rare genetic condition where the mitochondria—the energy-producing parts of cells—don’t work properly. This results in less energy for vital organs like the brain and muscles, leading to symptoms such as muscle weakness, neurological problems, seizures, and developmental delays. The severity varies among individuals and can affect movement, vision, hearing, and heart function. Since it’s caused by genetic mutations, it’s inherited and can be challenging to diagnose and treat. Management focuses on alleviating symptoms and improving quality of life, although there is currently no cure.