Congenital Lipoid Adrenal Hyperplasia Developed in a Brother and Sister / 대한주산의학회잡지
Korean Journal of Perinatology
;
: 191-195, 2010.
Artículo
en Coreano
| WPRIM
| ID: wpr-6944
ABSTRACT
Congenital lipoid adrenal hyperplasia (lipoid CAH) is an autosomal recessive disorder characterized by severe adrenal insufficiency. Clinical findings of patients are salt loss, hypoglycemia, pigmentation and male sex reversal. And also the baby with inadequate treatment may result in sudden death from adrenal crisis. We report the case of lipoid CAH developed in siblings with a brief review of associated literatures.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Pigmentación
/
Insuficiencia Suprarrenal
/
Muerte Súbita
/
Hermanos
/
Hiperplasia
/
Hipoglucemia
Límite:
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Korean Journal of Perinatology
Año:
2010
Tipo del documento:
Artículo
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