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Treatment of arginase deficiency revisited: guanidinoacetate as a therapeutic target and biomarker for therapeutic monitoring

  • Published:2014-05-10 Issue:10 Volume:56 Page:1021-1024
  • ISSN:0012-1622
  • Container-title:Developmental Medicine & Child Neurology
  • language:en
  • Short-container-title:Dev Med Child Neurol

Author:

Amayreh Wajdi1,Meyer Uta1,Das Anibh M1

Affiliation:

1. Department of Paediatrics; Clinic for Paediatric Kidney-, Liver- and Metabolic Diseases; Hannover Medical School; Hannover Germany

Publisher

Wiley

Subject

Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health

Reference15 articles.

1. The gene for human arginase (ARG1) is assigned to chromosome band 6q23;Sparkes;Am J Hum Genet,1986

2. Hyperargininemia due to liver arginase deficiency;Crombez;Mol Genet Metab,2005

3. Clinical, biochemical, and molecular spectrum of hyperargininemia due to arginase I deficiency;Scaglia;Am J Med Genet C Semin Med Genet,2006

4. Clinical features and neurologic progression of hyperargininemia;Carvalho;Pediatr Neurol,2012

5. Hyperargininemia presenting as persistent neonatal jaundice and hepatic cirrhosis;Braga;J Pediatr Gastroenterol Nutr,1997
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