Obesity; most common metabolic complication in Prader-Willi syndrome
Obesity and prader willi
(Sprache: Englisch)
Prader-Willi syndrome (PWS) is a genetic disorder due to loss of function of specific genes. In newborns, symptoms include weak muscles, poor feeding, and slow development. Beginning in childhood, the person becomes constantly hungry, which often leads to...
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Prader-Willi syndrome (PWS) is a genetic disorder due to loss of function of specific genes. In newborns, symptoms include weak muscles, poor feeding, and slow development. Beginning in childhood, the person becomes constantly hungry, which often leads to obesity and type 2 diabetes. Also, mild to moderate intellectual impairment and behavioural problems are typical. Often, the forehead is narrow, hands and feet are small, height is short, skin is light in colour, and most of the affected are unable to have children.
Autoren-Porträt von Eman Refaat Youness, Safinaz E. El Toukhy
Refaat Youness, EmanDr. Eman Refaat Youness, MD, Medical Biochemistry, Faculty of Medicine, Cairo university, Professor of medical Biochemistry, National Research centre, Egypt, Experienced in experimental design, clinical Researches, DNA, PCR,have a lot of international publications, member in international societies, Reviewer and editor in many journals.
Bibliographische Angaben
- Autoren: Eman Refaat Youness , Safinaz E. El Toukhy
- 2020, 56 Seiten, Maße: 22 cm, Kartoniert (TB), Englisch
- Verlag: Scholar's Press
- ISBN-10: 6138924576
- ISBN-13: 9786138924579
Sprache:
Englisch
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