Heidelberg Updates | Schaaf-Yang | United In Hope 2025
Автор: Foundation For Prader-Willi Research
Загружено: 2025-07-11
Просмотров: 294
Описание:
#SchaafYangSyndrome #UnitedInHope2025 #RareDiseaseResearch
Get the latest research updates from Heidelberg on Schaaf-Yang syndrome, shared at the United in Hope 2025 Conference.
This session highlights new discoveries about SYS biology, potential treatment strategies, and what’s next in the fight against this rare genetic disorder. Whether you're a parent, scientist, or advocate, this update will leave you informed—and hopeful.
Schaaf-Yang syndrome is caused by mutations in the MAGEL2 gene and is closely related to Prader-Willi syndrome. Learn more at https://www.fpwr.org/sys-home
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