A Case of True Hermaphroditism Masquerading as Testicular Tumor / 대한비뇨기과학회지
Korean Journal of Urology
;
: 1085-1087, 1999.
Artículo
en Coreano
| WPRIM
| ID: wpr-150594
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:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Trastornos del Desarrollo Sexual
/
Trastornos Ovotesticulares del Desarrollo Sexual
/
Genitales Masculinos
Límite:
Adolescente
/
Humanos
/
Masculino
/
Recién Nacido
Idioma:
Coreano
Revista:
Korean Journal of Urology
Año:
1999
Tipo del documento:
Artículo
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