One Case of the Prader-Willi Syndrome / 대한비뇨기과학회지
Korean Journal of Urology
;
: 630-632, 1981.
Artigo
em Coreano
| WPRIM
| ID: wpr-170719
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.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Síndrome de Prader-Willi
/
Células de Sertoli
/
Espermatogônias
/
Biópsia
/
Hiperfagia
/
Hipogonadismo
/
Deficiência Intelectual
/
Hipotonia Muscular
/
Obesidade
Idioma:
Coreano
Revista:
Korean Journal of Urology
Ano de publicação:
1981
Tipo de documento:
Artigo
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