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

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Journal of Inherited Metabolic Disease

Abstract

Congenital porto–left renal venous (PRV) shunt was found to be the cause of galactosaemia in four galactosaemic neonates detected by mass screening (Paigen method). The patients did not have hereditary galactosaemias and were diagnosed as having galactosaemia of unknown cause, because porto–systemic venous (PS) shunts had not been recognized. At the time of diagnosis, hypergalactosaemia was not severe (0.44–0.55 mmol/L; 8–10 mg/dl) and plasma concentration of total bile acids (TBA) did not suggest a PS shunt (46–50 μmol/L). However, slightly but consistently increased concentrations of galactose and TBA strongly suggested the presence of a PS shunt, and careful ultrasonographic investigation revealed PRV shunt. We conclude that PRV shunt should be suspected in patients with hypergalactosaemia of unknown cause.

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REFERENCES

  • Boon LM,Burrows PE,Paltiel HJ, et al (1996) Hepatic vascular anomalies in infancy: a twenty-seven-year experience. J Pediatr 129: 346–354.

    Google Scholar 

  • Gitzelmann R,Steinmann B (1973) Uridine diphosphate galactose 4-epimerase de¢ciency. Helv Paediatr Acta 28: 497–510.

    Google Scholar 

  • Gitzelmann R,Arbenz UV,Willi UV (1992) Hypergalactosemia and portosystemic encephalopathy due to persistence of ductus venosus Arantii. Eur J Pediatr 151: 564–568.

    Google Scholar 

  • Guariso G,Fiorio S,Altavilla G, et al (1998) Congenital absence of the portal vein associated with focal nodular hyperplasia of the liver and cystic dysplasia of the kidney. Eur J Pediatr 157: 287–290.

    Google Scholar 

  • Hansen RG,Mayes JS (1966) Galactose-1-phosphate uridyltransferase. Methods Enzymol 9: 713–718.

    Google Scholar 

  • Matsumoto T,Okano R,Sakura N, et al (1993) Hypergalactosemia in a patient with port-al-hepatic venous and hepatic arterio-venous shunts detected by neonatal screening. Eur J Pediatr 152: 990–992.

    Google Scholar 

  • Mizoguchi N,Eguchi T,Sakura N,Ueda K (1993) Erythrocyte galactokinase assays with high performance liquid chromatography. Clin Chim Acta 216: 145–151.

    Google Scholar 

  • Ono H,Mawatari H,Mizoguchi N,Eguchi T,Sakura N (1998) Clinical features and outcome of eight patients with intrahepatic porto-venous shunts detected in neonatal screening for galactosemia. Acta Paediatr 87: 631–634.

    Google Scholar 

  • Raskin NH,Price JB,Fishman RA (1964) Portal-systemic encephalopathy due to congenital intrahepatic shunts. N Engl J Med 270: 225–229.

    Google Scholar 

  • Sakura N,Mizoguchi N,Eguchi T, et al (1997) Elevated plasma bile acids in hypergalactosemic neonates: a diagnostic clue to portosystemic shunts. Eur J Pediatr 156: 716–718.

    Google Scholar 

  • Uchino T,Matsuda I,Endo F (1999) The long-term prognosis of congenital portosystemic venous shunt. J Pediatr 136: 254–256.

    Google Scholar 

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Mizoguchi, N., Sakura, N., Ono, H. et al. Congenital porto–left renal venous shunt as a cause of galactosaemia. J Inherit Metab Dis 24, 72–78 (2001). https://doi.org/10.1023/A:1005615023698

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  • DOI: https://doi.org/10.1023/A:1005615023698

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