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Prader-Willi syndrome |
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Prader-Willi syndrome [¦präd·ər ¦wil·ē ′sin‚drōm]
(medicine) A genetic disorder that is caused by defects on the paternally derived chromosome 15, causing mild mental retardation, neonatal hypotonia, hypogonadism, compulsive overeating, childhood onset obesity, and mild facial dysmorphism. Want to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit the webmaster's page for free fun content. |
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