Prader-Willi syndrome

(redirected from Willi, Heinrich)
Also found in: Dictionary, Medical.

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.
Mentioned in ?