Prader Willi Syndrome

What is Prader Willi syndrome?

Prader Willi syndrome is a chromosomal abnormality found in 1 of 10,000 to 25,000 births. It occurs due to a micro deletion on chromosome 15 caused by a defective gene from the father. When the defective gene comes from the mother it is called Angelman syndrome.download film Aardvark

What are the signs and cheap football jerseys symptoms of Prader Willi syndrome?

A baby with Prader Willi syndrome often presents as a breech delivery. Other signs and symptoms of Prader Willi syndrome include:

• no muscle strength (hypotonia) in newborn;
• feeding problems;
• low body temperature;
• small feet and hands (when compared to body size);
• no feeling of Cheap Ray Ban Sunglasses being full (leads to obesity in later years);
• narrow forehead;
• long face;
• almond-shaped eyes;
• mental retardation; and
• longer sleeping patterns.

How is Prader Willi syndrome treated?

There is no treatment for this condition as this is a genetic syndrome. These individuals will need a supportive environment and often live in a specialized home that is equipped to provide the required care.

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