PWS is the most common of the genetic disorders that cause life-threatening obesity in children. The syndrome affects many aspects of the person's life, including eating, behavior and mood, physical growth, and intellectual development.
PWS is the most common of the genetic disorders that cause life-threatening obesity in children. The syndrome affects many aspects of the person's life, including eating, behavior and mood, physical growth, and intellectual development.
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.
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: Use of special nipples or tubes for feeding difficulties. Difficulty in sucking is one of the most common symptoms of newborns with ...
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 ...
How do healthcare providers diagnose Prader-Willi syndrome (PWS)? In many cases of Prader-Willi syndrome, diagnosis is prompted by physical symptoms in the newborn.
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.
NICHD offers and links to information to help patients, families, and providers better understand Prader-Willi Syndrome and its effects and receive needed support.
The genetic disorder Fragile X syndrome, which results from mutations in a gene on the X chromosome, is the most commonly inherited form of developmental and intellectual disability.
