This document summarizes mitochondria and mitochondrial diseases. Mitochondria are structures within cells that convert energy from food into a form that cells can use, called ATP. Mitochondrial diseases can result from genetic mutations that affect mitochondria and disrupt energy production. Symptoms are wide-ranging but can include muscle and neurological problems. Causes include inherited genetic issues or random occurrences. While there is no cure, treatments focus on supplements, diet changes, and antioxidants to support mitochondrial function. The document specifically discusses how Parkinson's disease may be linked to mitochondrial dysfunction in the brain.