Research and Reports on Genetics

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Research and Reports on Genetics 44 7897 074717

Prader Willi Syndrome Scholarly Peer Review Journal

Syndrome Prader-Willi is a complex genetic disorder that affects many areas of the body. In childhood, this syndrome is characterized by low muscle tone, difficulty in eating, slow development, and delayed growth. Beginning in infancy, the individuals affected grow an insatiable appetite, leading to recurrent overeating and obesity. Typically , people with Prader-Willi syndrome have mild to moderate intellectual impairment and learning impairments. Behavioral issues are common including temperature outbursts, stubbornness, and compulsive behavior such as skin picking. Anomalies to the sleep may also occur. Additional features of this disorder include distinctive facial characteristics such as a high forehead, almond-shaped eyes and a triangular mouth; short stature; small hands and feet.

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