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- What causes Prader-Willi syndrome (PWS)? - NICHD
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 This part of the chromosome is called unstable because it is prone to being shuffled around by the cell's genetic machinery before the chromosome is passed on from parent to child
- Prader-Willi Syndrome (PWS) | NICHD - NICHD - Eunice Kennedy Shriver . . .
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 are the symptoms of Prader-Willi syndrome (PWS)?
The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria Pediatrics 108, e92 Retrieved on May 30, 2012, from https: pubmed ncbi nlm nih gov 11694676
- What are the treatments for Prader-Willi syndrome (PWS)?
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: Implications for imprint-switch models, genetic counseling, and prenatal diagnosis American Journal of Human Genetics, 63 , 170-180
- Prader-Willi Syndrome (PWS) - NICHD - Eunice Kennedy Shriver National . . .
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 This part of the chromosome is called unstable because it is prone to being shuffled around by the cell's genetic machinery before the chromosome is passed on from parent to child
- How do healthcare providers diagnose Prader-Willi syndrome (PWS . . . - NICHD
In many cases of Prader-Willi syndrome, diagnosis is prompted by physical symptoms in the newborn If a newborn is unable to suck or feed for a few days and has a "floppy" body and weak muscle tone, a health care provider may conduct genetic testing for Prader-Willi syndrome 1,2,3 Formal diagnostic criteria for recognizing Prader-Willi syndrome depend on the age of the individual-specifically
- NICHD Prader-Willi Syndrome Research Information
Prader-Willi syndrome encompasses a set of related conditions with a range of symptoms that affect eating and metabolism, growth, behavior, and intellectual development NICHD, part of the NIH within the U S Department of Health and Human Services, is one of many federal entities supporting research on Prader-Willi syndrome
- Prader-Willi Syndrome Resources | NICHD - NICHD - Eunice Kennedy . . .
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 Association (USA) This association is a leading patient advocacy group, providing support to individuals with PWS and their families
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