Prader-Willi Syndrome (PWS) comes with a range of physical, behavioural, and cognitive challenges, including mild to moderate intellectual disability, hyperphagia (an insatiable appetite), and compulsive… Read More »The Puzzle-Solving Strengths of Individuals with PWS
Prader-Willi Syndrome (PWS) is a rare genetic disorder that affects many aspects of a person’s life, including their physical health, behaviour, and metabolism. Finding effective… Read More »Can AI help us find new treatments for PWS?
Prader-Willi Syndrome (PWS) is a complex, genetic disorder that affects many aspects of a person’s health and development. Scientists are exploring new ways to treat… Read More »What are ER Chaperones and Could they Improve Treatment for Prader-Willi Syndrome
Prader-Willi Syndrome (PWS) affects many aspects of a person’s life, including their physical health and development. One of the challenges faced by adults with PWS… Read More »Can Growth Hormone slow down premature ageing in adults with PWS?
Prader-Willi Syndrome (PWS) and Congenital Myasthenic Syndrome-22 (CMS22) are two rare genetic disorders that, at first glance, might seem unrelated. However, recent research has uncovered… Read More »Exploring the Connection Between PWS and CMS22
What is Schaaf-Yang Syndrome?Schaaf-Yang Syndrome (or SYS) was first described by Dr Christian Schaaf in 2013. It is caused by a mutation or deletion in… Read More »Schaaf Yang Syndrome