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  • Casual Articles - Prader-Willi Syndrome - An Excessive Eating Disorder

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    as well as several other physical symptoms. The disorder oc
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    Prader-Willi Syndrome is a genetic disorder that occurs in approximately 1 in 15,000 live births. It can affect both genders, and all races and ethnic groups. It is characterized by excessive hunger, known as hyperphagia, mental retardation, as well as several other physical symptoms. The disorder occ
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    pproximately 1 in 15,000 live births. It can affect both genders, and all races and ethnic groups. It is characterized by excessive hunger, known as hyperphagia, mental retardation, as well as several other physical symptoms. The disorder oc
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    ders, and all races and ethnic groups. It is characterized by excessive hunger, known as hyperphagia, mental retardation, as well as several other physical symptoms. The disorder oc
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    excessive hunger, known as hyperphagia, mental retardation, as well as several other physical symptoms. The disorder oc
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    as well as several other physical symptoms. The disorder occurs when 7 genes on chromosome 15 are missing on the paternal chromosome.

    Prader-Willi Syndrome is currently diagnosed using genetic testing, especially in newborns with hypotonia, or very low muscle tone (also know as “floppy baby”).

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