Medical Dictionary

Prader–Willi syndrome

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noun Pra·der–Wil·li syndrome \ˈprä-dər-ˈvil-ē-\

Medical Definition of Prader–Willi syndrome

  1. :  a genetic disorder characterized by short stature, mental retardation, hypotonia, abnormally small hands and feet, hypogonadism, and uncontrolled appetite leading to extreme obesity

Biographical Note for prader–willi syndrome

Prader

,

Andrea

(1919–2001), and

Willi

,

Heinrich

(1900–1971), Swiss pediatricians. Prader was a professor of pediatrics in Zurich. Her articles and chapters in textbooks dealt with such topics as genetics, growth, endocrinology, and metabolism in children and adolescents. Prader and Willi first described the Prader-Willi syndrome in 1956. Cases of the disorder were not diagnosed in the United States until the 1960s.


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