Fulminant Hepatitis B and Neonatal Hepatitis with Galactosemia-Like Presentation

Haia Dyy , Walker FA Variability in the clinical manifestation of galactosemia. J Pediatr 1961; 59:872-88.

Monk AM , Mitchell Ajh , Milligan Dwa , et al. Diagnosis of classical galactosemia. Arch Dis Child 1977; 52:943-6.

Mowat AP Liver disorders in childhood. London: Butterworths, 1987: 171-3.

Balistreri WF , Schubert WK Liver disease in infancy and childhood. In: Schiff L , Schiff ER , (eds.) Disease of the liver. Philadelphia: JB Lippincott, 1987; 1137-1426.

Johnson PJ , McFarlane IG The laboratory investigation of liver disease. London: Bailliere Tindall, 1989: 55.

Gremse DA , Balistreri WF Neonatal Cholestasis. In: Textbook of gastroenterology and nutrition in infancy. Lebenthal E (ed.), Raven Press, Ltd, New York, 1989: 923-4.

Heuby JE , Daugherty CC Neonatal cholestasis: an approach for the practicing pediatrician. Curr Probl Pediatr, 20; 1990; 231-84.

Tanner S. Pediatric hepatology. Edinburgh: Churchill Livingstone, 1989: 105-8.

Alagille D. , Odievre M. Maladies du foie et des voies biliaires chez 1'enfant. Paris: Flammarion, 1978: 159-61.

Komrower GM Galactosemia - the experience of a generation . J Inher Metab Dis 1982: 96-104.

Tengstrom B. An intravenous galactose tolerance test with an enzymatic determination of galactose. A comparison with other diagnostic aids in hepatobiliary disease. Scand J Clin Lab Inv 1966; 18:132-42.

Sitzmann FC , Kaloud H. Biokinetics of galactose in the homozygotes and heterozygotes of both forms of galactosemia. Clin Chim Acta 1976; 72:343-52.

Wharton BA , Scott PH The newborn. In: Clayton BE , Rounds JM , eds. Chemical pathology and the sick child. Oxford and London: Blackwell, 1984: 7-72.

Ramsoe K. , Buck Andreasen P , Ranek L. Functioning liver mass in uncomplicated and fulminant acute B hepatitis. Scand J Gastroenterol 1980; 15:65-72.

Shiraki K. , Yoshihara BN , Sakurai M. Acute hepatitis B in infants born to carrier mothers with the antibody to hepatitis B e antigen. J Pediatr 1980; 97:768-70.

Delaplane D. , Yogev R. , Crussi F. , et al. Fatal hepatitis B in early infancy: the importance of identifying HBsAg positive pregnant women and providing immunoprophylaxis to their newborns. Pediatr 1983; 72:176-80.

Cordeiro Ferreira G. , Veiga M. , Po'I , et al. Hepatite fulminante chez un nourisson ne' de mere porteuse d' antigene desurface et d' anticorps "e" du virus de l'hepatite B. Helv Paediat Acta 1987; 42:41-4.

Vecchione R. , Russo R. , D' Armiento M. , et al. Eziologia della cholestasi del lattante in 54 casi osservati in Campania. Ital J Ped 1987; 5:71 (abstr).

Taylor CJ , Rattenbury JM , Allen JC , et al. Transient neonatal galactosemia. Arch Dis Child 1988; 63:1388-90

Segal S. Disorders of galactose metabolism. In: Stanbury JB , (ed.) The Metabolic Basis of Inherited Disease. New York: McGraw-Hill Book Company, 1989: 453-80.

Wallack J. Interpretation of diagnostic tests. Boston: Little Brown, 1978: 147.

Yu JS , Walker Smith JA , Burnard ED Neonatal hepatitis in premature infants simulating hereditary tyrosinosis . Arch Dis Child 1971; 46:306-9.

Willems C. , Heusden A. , Renson P. , et al. Hypertirosinemie avec hypermethioninemie neonatales dans un cas d'intolerance au fructose. Helv Paed Acta 1971; 26:467-81.

Hug G. , Chuck G. , Bowles B. Alpha-1-antitrypsin phenotype. Transient cathodal shift in serum of an infant girl with urinary cytomegalo virus and fatty liver. Pediatr Res 1982; 16:193-8.

Attenburrow AA Modification of the alpha-1-antitrypsin phenotype in neonatal hepatitis. Arch Dis Child 1985 ; 60:378-9.

Fishler K. , Coch R. , Donnel GN , et al. Developmental aspects of galactosemia from infancy to childhood . Clin Pediatr 1980; 19:38-44.