J Korean Pediatr Soc.  1980 Jul;23(7):590-597.

A Case of Prader-Willi Syndrome

Affiliations
  • 1Dept. of Pediatrics, Seoul Red Cross Hospital, Korea.
  • 2Dept. of Pediatrics, College of Medicine, Kyung Hee University, Korea.

Abstract

Prader-Willi syndrome is characterized by 1) hypotonia in the newborn infant 2) obesity which begins in childhood 3) short stature 4) typical facial features 5) secondary hypogonadism 6) juvenile diabetes mellitus of the maturity-onset type 7) mental retardation The true etiology of Prader-Willi syndrome is still unknown ; however, a hypothalamic disturbance has been postulated. We experienced a 9 year and 6 month old boy who revealed cryptorchidism, obesity, and mental retardation, whose picture was compatible with Prader-Willi syndrome.


MeSH Terms

Cryptorchidism
Diabetes Mellitus
Humans
Hypogonadism
Infant
Infant, Newborn
Intellectual Disability
Male
Muscle Hypotonia
Obesity
Prader-Willi Syndrome*
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