Gynecology and Reproductive Endocrinology

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Gynecology and Reproductive Endocrinology 44 7897 074717

Prader Willi Syndrome Impact Factor

Prader-Willi syndrome may be a genetic disease usually caused by the deletion of a neighborhood of chromosome 15 passed down by the daddy . the foremost common symptoms of Prader-Willi syndrome are behavioral problems, intellectual disability, and short stature. Hormonal symptoms include delayed puberty and constant hunger resulting in obesity. there's no cure for Prader-Willi syndrome but many patients will enjoy a supervised diet. Some symptoms are often treated with hormone therapy.

An extensive review of the literature was performed and interpreted within the context of clinical practice and regularly asked questions from referring physicians and families to incorporate the present status of the cause and diagnosis of the clinical, genetics and endocrine findings in PWS.

Updated information regarding the first diagnosis and management of people with Prader-Willi syndrome is vital for all physicians and can be helpful in anticipating and managing or modifying complications related to this rare obesity-related disorder.

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