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Three siblings with nonketotic hyperglycinaemia, mildly elevated plasma homocysteine concentrations and moderate methylmalonic aciduria

  • Published:2000-07 Issue:5 Volume:23 Page:520-522
  • ISSN:0141-8955
  • Container-title:Journal of Inherited Metabolic Disease
  • language:en
  • Short-container-title:J Inherit Metab Dis

Author:

Randak C.1,Röschinger W.1,Rolinski B.1,Hadorn H.-B.1,Applegarth D. A.23,Roscher A. A.1

Affiliation:

1. ; Department of Pediatrics, Dr. von Haunersches Kinderspital; Ludwig-Maximilians-Universität München; Lindwurmstrasse 4 Munich D-80337 Germany

2. ; Department of Pediatrics; University of British Columbia; Canada

3. ; Biochemical Diseases Laboratory; British Columbia's Children's Hospital; Vancouver B.C. Canada

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference6 articles.

1. Acute neonatal nonketotic hyperglycinemia: normal propionate and methylmalonate metabolism;Baumgartner;Pediatr Res,1975

2. Nonketotic hyperglycinemia with increased propionic acid excretion and hyperammonemia;Farriaux;N Engl J Med,1976

3. Effects of the metabolites of the branched-chain amino acids and cysteamine on the glycine cleavage system;Hayasaka;Biochem Int,1983

4. Nonketotic hyperglycinemia. Glycine accumulation due to absence of glycine cleavage in brain;Perry;N Engl J Med,1975
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