About The Medical Condition Syndrome, Prader-Willi
Find the definition of the medical term Syndrome, Prader-Willi. Syndrome, Prader-Willi defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.
Syndrome, Prader-Willi
| Syndrome, Prader-Willi Medical Condition |
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What's The Definition Of The Medical Condition Syndrome, Prader-Willi?
A chromosomal disorder associated with a deletion of the proximal portion of the long arm of chromosome 15 (15q11-q13) in the majority of affected individuals. The abnormalities occur exclusively on the paternally derived chromosome 15. Clinical manifestations include MENTAL RETARDATION, muscular hypotonia, OBESITY, hyperphagia, short stature, hypogonadism, strabismus, and hypersomnolence. (Menkes, Textbook of Child Neurology, 5th ed, p229)
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