About The Medical Condition Labhart-Willi-Prader-Fanconi Syndrome
Find the definition of the medical term Labhart-Willi-Prader-Fanconi Syndrome. Labhart-Willi-Prader-Fanconi Syndrome defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.
Labhart-Willi-Prader-Fanconi Syndrome
| Labhart-Willi-Prader-Fanconi Syndrome Medical Condition |
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What's The Definition Of The Medical Condition Labhart-Willi-Prader-Fanconi Syndrome?
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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