Three-year-old with tuberous sclerosis and PARDS receives life-saving care at Rainbow Children’s Hospital in Bengaluru.

Tuberous sclerosis complex is linked to a genetic mutation in TSC1 (on chromosome 9q34), [2] which produces hamartin, and in TSC2 (on chromosome 16p13.3), which produces tuberin. [3] ...

Sir David Suchet has spoken about his young grandson’s “very rare” and “incurable” condition, saying that he is “campaigning ...

The Tuberous Sclerosis Alliance (www.tsalliance.org) and the National Institutes of Arthritis, Musculoskeletal and Skin Diseases are two very useful resources. References ...

No medication worked. He has something called tuberous sclerosis, which is a genetic disorder that can affect all of your major organs,” Kerri Scott, Alex’s mom, said.

What You Need To Know 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.

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.