Prader-Willi Syndrome (PWS) is an unusual genetic condition with several physical, cognitive, and behavioural challenges. It typically occurs due to the loss of function of specific genes on chromosome 15.
PWS can arise from genetic mechanisms like deletions, imprinting defects, or uniparental disomy (where the individual inherits both copies from the parents).
This article will examine the Prader-Willi syndrome, its signs and symptoms, types, diagnosis, treatment, management, and the future outlook for affected people.