Tuberous sclerosis, also known as tuberous sclerosis complex, is a rare genetic condition that causes mainly non-cancerous (benign) tumours to develop in different parts of the body.
Prevalance of Tuberous sclerosis is reported to be less than 1 in 10,000 of population. Tuberous sclerosis is listed as a "rare disease" by the Office of Rare Diseases (ORD)
Specific medications may be prescribed for behaviour problems. Intervention programs including special schooling and occupational therapy may benefit individuals with special needs and developmental issues.
Current research in TSC includes: Identification of the TSC genes, DNA testing for TSC, Discovering the natural history of TSC, Understanding what goes wrong in TSC cells, Clinical trials of mTOR inhibitors etc..