Your browser doesn't support javascript.
loading
One Case of the Prader-Willi Syndrome / 대한비뇨기과학회지
Korean Journal of Urology ; : 630-632, 1981.
Article in Ko | WPRIM | ID: wpr-170719
Responsible library: WPRO
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.
Subject(s)
Key words
Full text: 1 Index: WPRIM Main subject: Prader-Willi Syndrome / Sertoli Cells / Spermatogonia / Biopsy / Hyperphagia / Hypogonadism / Intellectual Disability / Muscle Hypotonia / Obesity Language: Ko Journal: Korean Journal of Urology Year: 1981 Type: Article
Full text: 1 Index: WPRIM Main subject: Prader-Willi Syndrome / Sertoli Cells / Spermatogonia / Biopsy / Hyperphagia / Hypogonadism / Intellectual Disability / Muscle Hypotonia / Obesity Language: Ko Journal: Korean Journal of Urology Year: 1981 Type: Article