Prader-Willi Syndrome with Hypogonadism / 대한남성과학회지
Korean Journal of Andrology
;
: 85-87, 2011.
Artigo
em Coreano
| WPRIM
| ID: wpr-148322
ABSTRACT
Prader-Willi syndrome (PWS) is a rare genetic disease caused by a deletion or disruption of genes in chromosome 15. Commonly associated characteristics of this disorder include obesity, mental retardation, short stature, and hypogonadotropic hypogonadism. A 3-year-old-boy who initially presented hypoplastic scotum, small penis and bilateral cryptorchism was confirmed the diagnosis of PWS using of with genetic tests. Finally, he was taken bilateral orchiopexy.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Pênis
/
Síndrome de Prader-Willi
/
Cromossomos Humanos Par 15
/
Testes Genéticos
/
Criptorquidismo
/
Orquidopexia
/
Hipogonadismo
/
Deficiência Intelectual
/
Obesidade
Idioma:
Coreano
Revista:
Korean Journal of Andrology
Ano de publicação:
2011
Tipo de documento:
Artigo
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