Korean J Urol.  1981 Dec;22(6):630-632.

One Case of the Prader-Willi Syndrome

Affiliations
  • 1Department of Urology, Chung-Ang University, College of medicine, Seoul, korea.

Abstract

Prader-Willi syndrome is characterized by such as infantile hypotonia, mental retardation hyperphagia with obesity and hypogonadism. We experienced one case of so called Prader-Willi syndrome associated with hypogonadotrophic hypogonadism, hypomentia, hyperphagia with obesity and cryptochism. Testicular biopsy revealed predominant Sertoli cells, decreased spermatogonia and edematous stromal tissue.

Keyword

Prader-Willi syndrome

MeSH Terms

Biopsy
Hyperphagia
Hypogonadism
Intellectual Disability
Muscle Hypotonia
Obesity
Prader-Willi Syndrome*
Sertoli Cells
Spermatogonia
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