Welcome to my genomics communities and all other science nerds! 🧬🔬🩺 Greetings from beautiful Innsbruck, where I had the most fabulous time discussing #genomics #praderwillisyndrome #schaafyangsyndrome #mTORsignalling #iPSCs and #raredisease. Oh, and great skiing, too! ⛷️🚠🏔️

Further information, by country:

🌍https://ipwso.org/
🇮🇪https://pwsai.ie/
🇩🇪https://prader-willi.de/
🇬🇧https://www.pwsa.co.uk/
🇺🇸https://www.pwsausa.org/
🇩🇰https://prader-willi.de/
🇿🇦https://www.praderwilli.org.za/
🇸🇪http://prader-willi.se/
🇦🇺http://www.pws.org.au/
🇲🇾https://www.pwsamalaysia.org.my/
🇨🇳http://www.xpwilli.org/m/
🇮🇳http://www.ipwsa.com/
🇧🇷https://www.spwbrasil.com.br/
🇨🇱http://www.prader-willi.cl/
🇨🇦https://www.fpwr.ca/
🇫🇷https://www.prader-willi.fr/
🇮🇹https://www.praderwilli.it/

#PraderWilliSyndrome #PWS

A personal post: Here is some information about Prader-Willi syndrome.

https://ipwso.org/pws-information/what-is-pws/

PWS is a rare genetic disorder characterised by physical, behavioural, neurocognitive, and other dysfunctions.

Folks with PWS require 24-hour care supervision for life. For obvious reasons therefore, their families & carers require corresponding ongoing supports.

PWS affects c. 1 in 20,000 births. As such, while rare, there are many cases in every country every year.

#PraderWilliSyndrome #PWS