Pediatric Mitochondrial Diseases

Pediatric mitochondrial diseases are a group of genetic disorders that affect the mitochondria, which are the energy-producing structures in our cells. These diseases can impact various organs and systems, leading to symptoms like muscle weakness, developmental delays, and problems with movement or coordination. Because the mitochondria are crucial for energy production, children with these conditions may experience fatigue and organ dysfunction. Diagnosis often involves genetic testing and biochemical evaluations, and management focuses on alleviating symptoms and supporting overall health, as there is currently no cure for these complex disorders.