Welcome to the Tuberous Sclerosis 2000 Study page
Tuberous Sclerosis (TS) is a rare genetic disease that causes non-malignant tumours to grow in the skin, brain and other organs. The TS 2000 study is the first comprehensive longitudinal study of Tuberous Sclerosis (TS) with over 140 families participating nationwide and 2 research centres based in Cambridge and London. The study has recr
uited children as soon as possible after diagnosis in order to collect good quality data on early development. The TS 2000 study also aims to identify factors that help determine intellectual, cognitive, psychiatric, and medical outcomes. This page will keep you up to date on the latest developments with the study and also provides links to research and support on TS.