Obesity; most common metabolic complication in Prader¿Willi syndrome - Refaat Youness, Eman;El Toukhy, Safinaz E.
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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.

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Produktbeschreibung
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.
Autorenporträt
Dr. Eman Refaat Youness, MD, Medical Biochemistry, Faculty of Medicine, Cairo university, Assistant 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