| LC control no. | sh 85138450 |
|---|---|
| LC classification | RJ496.T8 |
| Topical heading | Tuberous sclerosis |
| Variant(s) | Bourneville disease Bourneville phakomatosis Bourneville--Pringle disease Bourneville--Pringle's disease Bourneville's disease Cerebral sclerosis Epiloia Sclerosis, Cerebral Sclerosis tuberosa Sclerosis, Tuberous |
| See also | Hamartoma Intellectual disability Phakomatoses |
| Found in | MeSH, June 13, 2018 (Tuberous sclerosis. Scope note (partial): Autosomal dominant neurocutaneous syndrome classically characterized by mental retardation; epilepsy; and skin lesions (e.g., adenoma sebaceum and hypomelanotic macules). Entry terms (partial list): Bourneville Disease; Bourneville Phakomatosis; Bourneville's Disease; Bourneville-Pringle Disease; Bourneville-Pringle's Disease; Cerebral Sclerosis; Epiloia; Phacomatosis, Bourneville; Sclerosis Tuberosa. Mapped to: Hamartoma; Neoplastic syndromes, Hereditary; Malformations of cortical development; Neurocutaneous syndromes; Heredodegenerative disorders, Nervous system) |
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