What causes Prader-Willi syndrome (PWS)? - NICHD What causes Prader-Willi syndrome (PWS)? Prader-Willi syndrome is caused by genetic changes on an "unstable" region of chromosome 15 that affects the regulation of gene expression, or how genes turn on and off
What are the treatments for Prader-Willi syndrome (PWS)? What are the treatments for Prader-Willi syndrome (PWS)? Parents can enroll infants with PWS in early intervention programs However, even if a PWS diagnosis is delayed, treatments are valuable at any age The types of treatment depend on the individual’s symptoms The healthcare provider may recommend the following:
NICHD Prader-Willi Syndrome Research Information NICHD Prader-Willi Syndrome Research Information Intellectual and developmental disabilities (IDDs), including Prader-Willi syndrome, are a primary focus of NICHD’s research Prader-Willi syndrome encompasses a set of related conditions with a range of symptoms that affect eating and metabolism, growth, behavior, and intellectual development
Prader-Willi Syndrome Resources - NICHD The Foundation for Prader-Willi Research The foundation sponsors research to eliminate the challenges of PWS Its website includes several resources for families of people with the syndrome MedlinePlus: Prader-Willi Syndrome This website, from the National Library of Medicine at NIH, offers information and links to additional details and services related to PWS Prader-Willi Syndrome
Experimental therapy for Prader-Willi syndrome shows promise in mice Drugs capable of activating silenced genes improve survival and growth outcomes in a mouse model of Prader-Willi syndrome (PWS), a rare and incurable childhood disease that can lead to life-threatening obesity