COLESTASIS EN EL LACTANTE PDF

Mazushicage Arch Dis Child, 75pp. Biochim Biophys Acta, 22pp. Neonatal cholestasis as the presenting feature in cystic fibrosis. Si continua navegando, consideramos que acepta su uso.

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Hospital Universitario Infantil La Paz. Figura 1. La base del tratamiento de este tipo de colestasis es el de la causa desencadenante. Todos los casos presentan un acusado retraso de talla y un prurito constante que condiciona una mala calidad de vida.

Todo ello es similar a los casos con defecto de FIC1, pero existen diferencias entre ellos que pueden orientar hacia uno u otro grupo. Es el caso de la galactosemia, tirosinemia o fructosemia. Hepatitis viral aguda. Hepatitis autoinmune.

No se ha podido delimitar con exactitud el papel de los autoanticuerpos detectados en dicha respuesta inflamatoria. Colangitis esclerosante primaria. Enfermedad de Wilson. Colecistitis calculosa o acalculosa. Late referral for biliary atresia, missed opportunities for efective surgery.

The changing pattern of diagnosis of infantile cholestasis. J Paediatr Child Health. The jaundiced baby. En Kelly DA ed. Diseases of the liver and biliary system in children.

Ed Blackwell Publishing. Neonatal giant cell hepatitis: Histological and etiological finding. Am J Surg Pathol. The course of neonatal cholestasis in congenital combined pituitary hormone deficiency. J Pediatr Metabol. Surgical disorders of the liver and bile ducts and portal hypertension. En: Kelly Deirdre A ed. Blackwell Publishing. Sokol RJ and Mack C. Etiopathogenesis of biliary atresia. Semin Liver Dis. Kelly D, Davenport M.

Current management of biliary atresia. Arch Dis Child. Chardot C and Serinet MO. Prognosis of biliary atresia: what can be further improved? J Pediatr. Steroids in biliary atresia: single surgeon, single centre, prospective study. J Hepatol. Hum Mutat.

Features of Alagille syndrome in 92 patients: frequency and relation to prognosis. Liver transplantation in children with Alagille syndrome: indications and outcome. Pediatr Transplant.

Outcome of liver disease in children with Alagille syndrome: a study of patients. Hierro, P. Colestasis infantiles y transportadores biliares. Gastroenterol Hepatol. The natural history of liver disease in alphaantitrypsin deficient children. Acta Paediatr Scand. Whitington PF1. Gestational alloimmune liver disease and neonatal hemochromatosis. Mieli-Vergani G, Vergani D. Autoimmune paediatric liver disease.

World J Gastroenterol. Kelly DA. Preventing parenteral nutrition liver disease. Early Hum Dev. Epidemiology of liver disease in cystic fibrosis: a longitudinal study. Re-evaluation of the diagnostic criteria for Wilson disease in children with mild liver disease.

No consanguinidad. Embarazo normal. Peso: 3. A los dos meses, presenta ITU por E. Hipovitaminosis severa. Abdomen: hepatomegalia a 3 cm de consistencia normal, no esplenomegalia. No ascitis.

No hernias. AC y P: normal. GGT: Alfa-1antitripsina: Normal. Resto normal. Histologia: colestasis.

CYBERSEMIOTICS WHY INFORMATION IS NOT ENOUGH PDF

Colestasis neonatal

Hospital Universitario Infantil La Paz. Figura 1. La base del tratamiento de este tipo de colestasis es el de la causa desencadenante. Todos los casos presentan un acusado retraso de talla y un prurito constante que condiciona una mala calidad de vida.

BERLINER PLATZ 1 NEU ED LANGENSCHEIDT PDF

COLESTASIS EN EL LACTANTE PDF

Liver diseases in children, 2nd ed, pp. A disease or a phenotype. Recommendations for management of liver and biliary tract disease in Cystic Fibrosis. Full text is only aviable in PDF. Alpha-feto-protein during development and in disease. An Esp Pediatr, 28pp.

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