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Prader-Willi syndrome. | Journal of Medical Genetics
- https://jmg.bmj.com/content/34/11/917
- Prader-Willi syndrome is a complex disorder affecting multiple systems with many manifestations relating to hypothalamic insufficiency. Major findings …
Prader-Willi Syndrome | American Journal of Psychiatry
- https://ajp.psychiatryonline.org/doi/full/10.1176/ajp.155.9.1265
SUN-604 U.S. Prevalence & Mortality of Prader-Willi …
- https://academic.oup.com/jes/article/4/Supplement_1/SUN-604/5834046
- Prader-Willi syndrome (PWS) is a complex developmental genetic disorder associated with hypotonia, poor feeding in neonates, onset of hyperphagia in early …
Prader Willi syndrome: endocrine updates and new …
- https://journals.lww.com/co-endocrinology/Abstract/2020/02000/Prader_Willi_syndrome__endocrine_updates_and_new.11.aspx
- Prader Willi syndrome is characterized not only by hyperphagia frequently resulting in obesity, but also by endocrine dysfunction across a variety of axes. This article reviews …
Health Supervision for Children With Prader-Willi Syndrome
- https://publications.aap.org/pediatrics/article/127/1/195/30016/Health-Supervision-for-Children-With-Prader-Willi
- Prader-Willi syndrome provides an excellent example of how early diagnosis and management can improve the long-term outcome for some genetic disorders. This …
Requirements for improving health and well-being of …
- https://pubmed.ncbi.nlm.nih.gov/31257692/
- Prader-Willi syndrome (PWS) is a rare genetic condition with multi-system involvement. The literature was reviewed to describe neurodevelopment and the behavioural …
Prader‐Willi syndrome: Current understanding of cause …
- https://onlinelibrary.wiley.com/doi/abs/10.1002/ajmg.1320350306
- Prader-Willi syndrome (PWS) is characterized by hypotonia, obesity, hypogonadism, short stature, small hands and feet, mental deficiency, a characteristic face, and an interstitial …
Approach to the Child with Prader-Willi Syndrome | The …
- https://academic.oup.com/jcem/article/97/11/3837/2836373
- PWS has a prevalence of 1/10,000 to 1/30,000 individuals and is characterized by poor feeding in infancy often associated with failure to thrive, …
The Italian registry for patients with Prader–Willi syndrome
- https://ojrd.biomedcentral.com/articles/10.1186/s13023-023-02633-5
- Prader–Willi syndrome (PWS) is a rare and complex genetic disease, with numerous implications on metabolic, endocrine, neuropsychomotor systems, and with …
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