A Case of True Hermaphroditism Masquerading as Testicular Tumor / 대한비뇨기과학회지
Korean Journal of Urology
; : 1085-1087, 1999.
Artigo
em Coreano
| WPRIM (Pacífico Ocidental)
| ID: wpr-150594
Biblioteca responsável:
WPRO
ABSTRACT
True hermaphroditism represents the rarest of all intersex disorders. The condition is defined by the presence of both ovarian and testicular tissue in the same individual. True hermaphroditism is usually diagnosed during the newborn period in the course of evaluating ambiguous genitalia. We present an unusual case of a 15-year-old boy with phenotypically normal male genitalia and bilaterally descended ovotestis, who was seen for evalution of intermittent scrotal swelling and pain.
Texto completo:
Disponível
Base de dados:
WPRIM (Pacífico Ocidental)
Assunto principal:
Transtornos do Desenvolvimento Sexual
/
Transtornos Ovotesticulares do Desenvolvimento Sexual
/
Genitália Masculina
Limite:
Adolescente
/
Humanos
/
Masculino
/
Recém-Nascido
Idioma:
Coreano
Revista:
Korean Journal of Urology
Ano de publicação:
1999
Tipo de documento:
Artigo