Tuberous sclerosis

Hereditary disease characterized by seizures, intellectual disability, developmental delay, and skin and ocular lesions. First signs usually occur during infancy or childhood but in rare cases may not occur until 2nd or 3rd decade.

Also known as: Bourneville disease, Bourneville syndrome, Bourneville's disease, Bourneville's syndrome, TSC, epiloia, tuberous sclerosis, tuberous sclerosis complex

75 clinical trials for this condition and its sub-types, 41 tagged with Tuberous sclerosis itself.