The changing pattern of diagnosis of infantile cholestasis

Journal of Paediatrics and Child Health

Volumn 37, Issue 1, 2001, Pages 47-50

  Stormon, M O ^a   Dorney, S F A ^a   Kamath, K R ^a   O'Loughlin, E V ^a   Gaskin, K J ^a  

^a CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

Author keywords

Bile duct hypoplasia; Biliary obstruction; Cholestasis; Genetic metabolic disease; Liver disease; Neonatal

Indexed keywords

ARTICLE; BILE DUCT OBSTRUCTION; BILIARY TRACT DISEASE; CHOLESTASIS; GENETIC DISORDER; HUMAN; HYPOPLASIA; INFANT; INFANT DISEASE; LIVER DISEASE; MAJOR CLINICAL STUDY; METABOLIC DISORDER; PARENTERAL NUTRITION; PRIORITY JOURNAL; TOTAL PARENTERAL NUTRITION;

AGE OF ONSET; CHOLESTASIS; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; INFECTION; MALE; METABOLISM, INBORN ERRORS; NEW SOUTH WALES; PARENTERAL NUTRITION, TOTAL; RETROSPECTIVE STUDIES;

EID: 0035115618     PISSN: 10344810     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1440-1754.2001.00613.x     Document Type: Article

References (18)

1. Hepatitis syndrome in infancy - An epidemiological survey with 10 year follow up
2. Studies of the aetiology of neonatal hepatitis and biliary atresia
3. Liver disease in infancy: A 20 year perspective
4. Form of hepatitis in the neonatal period simulating biliary atresia
5. Outcome of surgery for biliary atresia
6. Liver disease in alpha-1-antitrypsin deficiency detected by screening of 200 000 infants
7. Liver disease in children with PiZZ alpha1-antitrypsin deficiency
8. Neonatal cholestasis as the presenting feature in cystic fibrosis
9. Neonatal cholestasis, hypoglycaemia and congenital hypopituitarism
10. Cholestatic jaundice and congenital hypopituitarism
11. Idiopathic neonatal iron storage involving the liver, pancreas, heart and endocrine and exocrine glands
12. Perinatal hemochromatosis: Entity or end result?
13. Liver disease in association with neonatal lupus erythematosus
14. Evidence for defective primary bile acid secretion in children with progressive familial intrahepatic cholestasis (Byler disease)
15. Normal serum X-glutamyl-transpeptidase activity identifies groups of infants with idiopathic cholestasis with poor prognosis
16. Sepsis due to Eschericia coli in neonates with galactosemia
17. Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): A review of 80 cases
18. Extrahepatic biliary atresia (EHBA) in Australia 1993-6