Epub 2015 Apr 1. de Vries PJ, Belousova E, Benedik MP, Carter T, Cottin V, Curatolo P, Dahlin M, D'Amato L, Beaure d'Augères G, Ferreira JC, Feucht M, Fladrowski C, Hertzberg C, Jozwiak S, Lawson JA, Macaya A, Marques R, Nabbout R, O'Callaghan F, Qin J, Sander V, Sauter M, Shah S, Takahashi Y, Touraine R, Youroukos S, Zonnenberg B, Kingswood JC, Jansen AC; TOSCA Investigators. Epub 2013 Feb 26. Zimmer TS, Broekaart DWM, Gruber VE, van Vliet EA, Mühlebner A, Aronica E. Front Neurol. Previous. 2017 Jun 9;6:F1000 Faculty Rev-859. By submitting your comment, and other materials (collectively referred to as a "Submission") to MedicineNet, you grant MedicineNet permission to use, copy, transmit, publish, display, edit and modify your Submission in connection with its Web site. ... Tuberous Sclerosis Complex Natural History Database is funded by Tuberous Sclerosis Alliance. Notably, the difference between the median depression score for men and women was statistically significant with men scoring higher than women (P = 0.02). Lung and kidney tumors are more likely to develop in adulthood. Autism was diagnosed in 23% and was associated with epilepsy (P < 0.001), particularly with epilepsy onset at age less than two years (P = 0.02) but not with genotype (P = 0.06). Tuberous sclerosis complex (TSC) is a rare multisystem autosomal dominant genetic disease that causes non-cancerous tumours to grow in the brain and on other vital organs such as the kidneys, heart, liver, eyes, lungs and skin.A combination of symptoms may include seizures, intellectual disability, developmental delay, behavioral problems, skin abnormalities, lung disease, and kidney disease. The majority of these tumors are benign, but they can significantly impact your child’s health and development. Tuberous Sclerosis Complex (TSC) is a hereditary disorder which causes benign non-invasive lesions on any organ within the human body. Tuberous sclerosis (TWO-bur-uhs skluh-ROH-sis), also called tuberous sclerosis complex, is an uncommon genetic disorder that causes noncancerous (benign) tumors — unexpected overgrowths of normal tissue — to develop in many parts of the body. ScienceDirect ® is a registered trademark of Elsevier B.V. ScienceDirect ® is a registered trademark of Elsevier B.V. Please enable it to take advantage of the complete set of features! * Screen Name will appear next to the published comment. 2020 Sep 17;11:1028. doi: 10.3389/fneur.2020.01028. Keywords: Neither parents have it. 2018 Sep 10;13(1):157. doi: 10.1186/s13023-018-0901-8. 2013 Nov;31(7):667-78. doi: 10.1016/j.ijdevneu.2013.02.008. Bolton PF, Clifford M, Tye C, Maclean C, Humphrey A, le Maréchal K, Higgins JN, Neville BG, Rijsdjik F; Tuberous Sclerosis 2000 Study Group, Yates JR. Psychol Med. Some of the first signs are seizures and spots on the skin. Results: It may be caused by mutations in genes TSC1 or TSC2. The authors appreciatively acknowledge the support of the Tuberous Sclerosis Alliance and the members of the TSC community who participated in this survey. HHS Information on 35 adults was gathered using four questionnaires: Epworth Sleepiness Scale (ESS), Sleep and … Find out how Tuberous Sclerosis can affect your mood. © 2018 Elsevier Inc. All rights reserved. NLM Skin abnormalities are present in all cases of tuberous sclerosis. Funding: This work was supported by the UT Tuberous Sclerosis Complex Center Endowment Fund. Attention-deficit/hyperactivity disorder (age greater than four years) was diagnosed in 18% and was associated with epilepsy (P < 0.001), but genotype made no difference. 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