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Neonatal Cholestasis Associated with Congenital Hypopituitarism / 대한소아소화기영양학회지
Korean Journal of Pediatric Gastroenterology and Nutrition ; : 199-205, 2002.
Article Dans Coréen | WPRIM | ID: wpr-112956
ABSTRACT
Congenital hypopituitarism is a possible cause of neonatal cholestasis, but the mechanism is still unknown. The pathogenesis of cholestasis may be due to hormone deficiency, which has effects on the physiological maturation of bile acid synthesis and transport. We experienced a case presenting with cholestasis and recurrent hypoglycemia associated with congenital hypopituitarism. Cholestasis resolved with thyroxine and hydrocortisone replacement therapy
Sujets)

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Thyroxine / Bile / Hydrocortisone / Cholestase / Hypoglycémie / Hypopituitarisme langue: Coréen Texte intégral: Korean Journal of Pediatric Gastroenterology and Nutrition Année: 2002 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Thyroxine / Bile / Hydrocortisone / Cholestase / Hypoglycémie / Hypopituitarisme langue: Coréen Texte intégral: Korean Journal of Pediatric Gastroenterology and Nutrition Année: 2002 Type: Article