Tuberous Sclerosis is a genetic disorder that causes non-cancerous tumors to form in various organs, particularly the brain, skin, heart, and kidneys. These tumors can lead to a range of symptoms, including seizures, developmental delays, and skin abnormalities. The condition is caused by mutations in the TSC1 or TSC2 genes, which are responsible for regulating cell growth. Diagnosis often involves imaging tests, skin examinations, and genetic testing. While there is no cure for Tuberous Sclerosis, treatments are available to manage symptoms and complications. Early intervention and regular monitoring can significantly improve the quality of life for those affected.