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Tuberous sclerosis

MONDO:0001734

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

74 clinical trials for this condition and its sub-types.

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Sub-types

Tuberous sclerosis 1 (29) Tuberous sclerosis 2 (2)

Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Inherited disease susceptibility (69) Hereditary neoplastic syndrome (57) Syndromic disease (24) Human disease (14) Neoplastic disease or syndrome (6) Hereditary neurological disease (5) Disease susceptibility (3)
Trials to join now! 36 Not yet recruiting 4 Not yet finished but already full! 18 Completed 11 Terminated 5
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