- Rare genetic condition
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Prader-Willi syndrome - Symptoms and causes - Mayo Clinic
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. People with Prader-Willi syndrome want to eat all the time because they never feel full. This is called hyperphagia. As a … 展开
Symptoms of Prader-Willi syndrome, which can vary, slowly change over time from childhood to adulthood. 展开
A child with an error in one or more genes in chromosome 15 is at the highest risk of getting Prader-Willi syndrome. For example, one of the genes … 展开
Prader-Willi syndrome is a genetic condition that is caused by an error in one or more genes. Although it's not known exactly what causes … 展开
- Obesity-related complications
- In addition to being hungry all the time, people with Prader-Willi syndrome have …
- Complications of not making enough hormones
- Complications that come fr… 展开
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. In newborns, symptoms include weak muscles, poor feeding, and slow development. Beginning in childhood, those affected become constantly hungry, which often leads to obesity and type 2 diabetes. Mild to moderate intellectual impairment and behavioral problems are …
Wikipedia · CC-BY-SA 许可下的文字Prader-Willi Syndrome: Symptoms & Causes - Cleveland Clinic
Prader-Willi syndrome is a rare genetic condition that affects metabolism, body and behavior. Learn about the symptoms, causes, diagnosis, treatment and complications of this condition …
What Is Prader-Willi Syndrome? - Symptoms and Causes - PWSA
Prader-Willi syndrome - MedlinePlus
Prader-Willi syndrome is caused by the loss of function of genes on chromosome 15, which affects many parts of the body. It is characterized by weak muscle tone, feeding difficulties, poor growth, delayed development, extreme hunger, …
Prader-Willi Syndrome: Characteristics, Complications, …
2024年4月12日 · Prader-Willi syndrome is a genetic disorder caused by changes to chromosome 15. It affects growth, behavior, and learning and requires continual management to avoid potentially life threatening ...
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Prader-Willi syndrome - NHS
Prader-Willi syndrome is a rare genetic condition that affects growth, appetite, learning and behaviour. It's caused by some missing genetic material on chromosome 15 and can be …
Prader-Willi Syndrome - Clinical Genetics, Diagnosis and …
Prader-Willi syndrome (PWS) is a complex neurodevelopmental disorder characterized by infantile hypotonia, poor suck and feeding difficulty, short stature with small hands and feet, …
Understanding Prader-Willi Syndrome: Key Traits, Associated …
2024年12月19日 · Prader-Willi Syndrome (PWS) is a genetic disorder resulting from the loss of function of genes on chromosome 15, leading to physical, cognitive, and behavioral …
Prader-Willi Syndrome - GeneReviews® - NCBI Bookshelf
1998年10月6日 · Prader-Willi syndrome (PWS) is a complex, multisystem disorder characterized by neonatal hypotonia with poor suck and poor weight gain without nutritional support, developmental delay, mild cognitive impairment, …
