A Case of 5 alpha-reductase Deficiency in Infancy / 대한소아내분비학회지
Journal of Korean Society of Pediatric Endocrinology
;
: 96-101, 1998.
Artigo
em Coreano
| WPRIM
| ID: wpr-125350
ABSTRACT
5 alpha-reductase deficiency resulting in male pseudohermaphroditism is a rare disease characterized by clitoral-like phallus, bifid scrotum, urogenital sinus, testis cited in labioscrotal folds. Evaluation of plasma T/DHT ratios in infancy, particularly after hCG stimulation of the testes and elevated urinary tetrahydrocortisol (THF) to 5 alpha-tetrahydrocortisol(5 alpha-THF) ratios provide a valuable dianostic test for 5 alpha-reductase deficiency. We report one case of 5 alpha-reductase deficiency who were presented with ambiguous genitalia and elevated T/DHT ratio before and after hCG stimulation.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Plasma
/
Escroto
/
Transtornos do Desenvolvimento Sexual
/
Testículo
/
Tetra-Hidrocortisol
/
Doenças Raras
/
Colestenona 5 alfa-Redutase
/
Transtorno 46,XY do Desenvolvimento Sexual
Idioma:
Coreano
Revista:
Journal of Korean Society of Pediatric Endocrinology
Ano de publicação:
1998
Tipo de documento:
Artigo
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