MELAS Syndrome

MELAS Syndrome, short for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes, is a rare genetic disorder that affects how the body produces energy. It primarily impacts the brain and muscles, leading to symptoms such as weakness, seizures, severe headaches, and episodes resembling strokes. The condition is caused by mutations in mitochondrial DNA, which is essential for energy production in cells. MELAS typically appears in childhood or early adulthood and can lead to progressive health issues. Management focuses on alleviating symptoms and supporting affected individuals, as there is currently no cure.