About TSC
Tuberous Sclerosis Complex (TS, or TSC) is a genetic, neurological condition distinguished by lesions of the skin and central nervous system, tumor growth, and seizures (epilepsy). Effects of the disease vary greatly, some cases are so mild they may go undiagnosed; others may experience developmental delay, autism, or mental retardation. In addition to the impacts of TS on the brain, it can also affect the heart, eyes, skin, lungs, and kidneys.
Estimates as to the incidence of TS put it at about 1/6,000 births; 50,000 people in the US, roughly one million worldwide. Although typically unheard of in the general population, TS is about as common as ALS and Hemophilia. TS occurs equally in males/females, and all races and ethnic groups. Only one of the two identified TS genes needs to be present to have the disorder. Even though TS is a genetic disorder, fully two-thirds of diagnosed cases are thought to be spontaneous mutations, which means that neither parent had the disorder present. The cause(s) of the mutation are unknown, there is no cure, and no way to predict the severity of the disease.
The lives of individuals with TSC, and their families, can be greatly enhanced by programs such as those offered by each of our three beneficiaries. The funds raised by Team Tamara will fund treatment programs, research, and awareness campaigns.
