News

The tuberous sclerosis clinic accepts referrals from primary care providers and pediatric specialists from the United States and internationally. To make a referral, there are three options: Call us ...
In an attempt to explain this gap in our understanding, Knoblich’s team generated cerebral organoids from people with TSC2 mutations to study tuberous sclerosis. The team utilized an in vitro human ...
Althea Grace dealt with her baby's diagnosis of tuberous sclerosis complex while competing on American Idol, managing her daughter's medical needs without giving up on her dreams Susan Young is a ...
Tuberous sclerosis complex is linked to a genetic mutation in TSC1 (on chromosome 9q34), which produces hamartin, and in TSC2 (on chromosome 16p13.3), which produces tuberin.
Tuberous sclerosis is a rare genetic condition that causes mainly benign tumours to develop in different parts of the body, such as the brain, heart, and lungs.
"Tuberous sclerosis complex is a genetic, or sporadic, disorder that affects multiple systems in the body and is highly associated with epilepsy -- about 80% of people have epilepsy -- and autism ...
The Step Forward to Cure TSC Walk Tamp pushes for tuberous sclerosis complex (TSC) awareness and funding. It's happening Saturday at MacFarlane Park in Tampa at 10 a.m.
A total of 13 pediatric patients aged 6 years to 17 years received Hyftor in the phase 3 study, along with 48 participants aged 3 years to 17 years in the 104-week open label safety trial.
SILVER SPRING, Md., May 7, 2025 /PRNewswire/ -- On May 15, the TSC Alliance® will join tuberous sclerosis complex (TSC) organizations around the world to observe the 13th Annual TSC Global ...