Congenital porto-left renal venous shunt as a cause of galactosaemia
Author:
Affiliation:
1. Department of Pediatrics; Japan
2. ; Department of Radiology; Hiroshima University School of Medicine; Hiroshima
3. Hiroshima City Clinical Research Center; Hiroshima Japan
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005615023698/fullpdf
Reference11 articles.
1. Hepatic vascular anomalies in infancy: a twenty-seven-year experience;Boon;J Pediatr,1996
2. Uridine diphosphate galactose 4-epimerase de¢ciency;Gitzelmann;Helv Paediatr Acta,1973
3. Hypergalactosemia and portosystemic encephalopathy due to persistence of ductus venosus Arantii;Gitzelmann;Eur J Pediatr,1992
4. Congenital absence of the portal vein associated with focal nodular hyperplasia of the liver and cystic dysplasia of the kidney;Guariso;Eur J Pediatr,1998
5. Galactose-1-phosphate uridyltransferase;Hansen;Methods Enzymol,1966
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