Congenital porto-left renal venous shunt as a cause of galactosaemia

Journal of Inherited Metabolic Disease

Volumn 24, Issue 1, 2001, Pages 72-78

  Mizoguchi, N ^a   Sakura, N ^a   Ono, H ^a   Naito, K ^b   Hamakawa, M ^c  

^a Department of Pediatrics ^*  (Japan)

^b HIROSHIMA UNIV SCHOOL OF MEDICINE   (Japan)

^c Association Clinical Laboratory Center   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BILE ACID; GALACTOSE;

ARTICLE; CASE REPORT; DISEASE SEVERITY; ECHOGRAPHY; FEMALE; GALACTOSEMIA; HUMAN; MALE; MASS SCREENING; NEWBORN; NEWBORN SCREENING; PORTOSYSTEMIC ANASTOMOSIS;

FEMALE; GALACTOSEMIAS; HEART DEFECTS, CONGENITAL; HUMANS; INFANT; INFANT, NEWBORN; MALE; PORTAL VEIN; RENAL VEINS; VASCULAR FISTULA;

EID: 0035106292     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005615023698     Document Type: Article

References (11)

1. Hepatic vascular anomalies in infancy: A twenty-seven-year experience
2. Uridine diphosphate galactose 4-epimerase deficiency
3. Hypergalactosemia and portosystemic encephalopathy due to persistence of ductus venosus Arantii
4. Congenital absence of the portal vein associated with focal nodular hyperplasia of the liver and cystic dysplasia of the kidney
5. Galactose-1-phosphate uridyltransferase
6. Hypergalactosemia in a patient with portal-hepatic venous and hepatic arterio-venous shunts detected by neonatal screening
7. Erythrocyte galactokinase assays with high performance liquid chromatography
8. Clinical features and outcome of eight patients with intrahepatic porto-venous shunts detected in neonatal screening for galactosemia
9. Portal-systemic encephalopathy due to congenital intrahepatic shunts
10. Elevated plasma bile acids in hypergalactosemic neonates: A diagnostic clue to portosystemic shunts
11. The long-term prognosis of congenital portosystemic venous shunt