Prader-Willi syndrome - Symptoms and causes - Mayo Clinic
2024年11月14日 · Prader-Willi (PRAH-dur VIL-e) syndrome is a rare genetic condition that leads to physical, mental and behavioral problems. A key feature of Prader-Willi syndrome is a sense of being hungry all the time.
Prader–Willi syndrome - Wikipedia
Prader–Willi syndrome (PWS) is a rare genetic disorder caused by a loss of function of specific genes on chromosome 15. [2] In newborns, symptoms include weak muscles, poor feeding, and slow development. [2] Beginning in childhood, those affected become constantly hungry, which often leads to obesity and type 2 diabetes. [2]
Prader-Willi Syndrome: Symptoms & Causes - Cleveland Clinic
Prader-Willi syndrome (PWS) is a rare genetic condition that affects your child’s metabolism and causes changes to their body and behavior. They have severe low muscle tone and poor feeding during early infancy, followed by a tremendous appetite that develops between 2 …
Prader-Willi Syndrome - StatPearls - NCBI Bookshelf
2024年2月26日 · Prader-Willi syndrome is a rare and complex genetic disorder that impacts the metabolic, endocrine, and neurologic systems. The syndrome manifests with severe hypotonia and feeding difficulties during the early years of life, leading to global developmental delays.
Prader-willi syndrome | About the Disease | GARD
A rare genetic, neurodevelopmental syndrome characterized by hypothalamic-pituitary dysfunction with severe hypotonia and feeding deficits during the neonatal period followed by an excessive weight gain period with hyperphagia with a risk of severe obesity during childhood and adulthood, learning difficulties, deficits of social skills and behav...
Prader-Willi syndrome - MedlinePlus
Prader-Willi syndrome is a complex genetic condition that affects many parts of the body. In infancy, this condition is characterized by weak muscle tone (hypotonia), feeding difficulties, poor growth, and delayed development.
Prader-Willi Syndrome (PWS) - NICHD - Eunice Kennedy Shriver ...
2012年6月13日 · 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.