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Autism and Epilepsy in Tuberous Sclerosis

Tuberous Sclerosis (Complex). 1 in 10,00040% inherited autosomal dominant genetic disorder60% spontaneous mutationTSC1 gene (9q34) 20% -hamartinTSC2 gene (16p13) 80% -tuberincharacterised by hamartomas affecting many organs (90% cerebral involvement)Epilepsy in 80%. . . Proteins control cell

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Autism and Epilepsy in Tuberous Sclerosis

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    1. Autism and Epilepsy in Tuberous Sclerosis Dr. Ayla Humphrey Consultant Clinical Psychologist Autism Research Centre Cambridge Tuberous Sclerosis Clinic Developmental Psychiatry University of Cambridge

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