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.
Key words
Full text:
1
Index:
WPRIM
Main subject:
Prader-Willi Syndrome
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Sertoli Cells
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Spermatogonia
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Biopsy
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Hyperphagia
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Hypogonadism
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Intellectual Disability
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Muscle Hypotonia
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Obesity
Language:
Ko
Journal:
Korean Journal of Urology
Year:
1981
Type:
Article