Literature DB >> 23430558

Case Report of Argininemia: The Utility of the Arginine/Ornithine Ratio for Newborn Screening (NBS).

Allison Jay1,2, Mary Seeterlin3, Eleanor Stanley3, Robert Grier4.   

Abstract

We describe a case of Argininemia detected by Michigan Newborn Screening (NBS). The Secretary's Advisory Committee on Heritable Disorders in Newborns and Children recommends that every MS/MS newborn screening program include Argininemia as part of their uniform screening panel. While affected infants will be detected by this testing, Arginine levels may take time to accumulate. Thus, some infants may not be detected by this methodology and early sample collection. In Michigan, since initiating testing for Argininemia in 2006, there has been workup of 23 cases for elevated Arginine identified by NBS, with one case identified as affected. We report this affected case. Subsequently, the Arginine/Ornithine ratio was calculated for all cases and was found to be informative with respect to predicting whether a patient is affected by Argininemia.

Entities:  

Year:  2012        PMID: 23430558      PMCID: PMC3565661          DOI: 10.1007/8904_2012_190

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  2 in total

Review 1.  Clinical, biochemical, and molecular spectrum of hyperargininemia due to arginase I deficiency.

Authors:  Fernando Scaglia; Brendan Lee
Journal:  Am J Med Genet C Semin Med Genet       Date:  2006-05-15       Impact factor: 3.908

Review 2.  Hyperargininemia due to liver arginase deficiency.

Authors:  Eric A Crombez; Stephen D Cederbaum
Journal:  Mol Genet Metab       Date:  2004-12-19       Impact factor: 4.797

  2 in total
  5 in total

1.  Natural history of arginase 1 deficiency and the unmet needs of patients: A systematic review of case reports.

Authors:  Aseel Bin Sawad; Arti Pothukuchy; Mark Badeaux; Victoria Hodson; Gillian Bubb; Kristina Lindsley; Jennifer Uyei; George A Diaz
Journal:  JIMD Rep       Date:  2022-03-25

2.  The Newborn Screening Quality Assurance Program at the Centers for Disease Control and Prevention: Thirty-five Year Experience Assuring Newborn Screening Laboratory Quality.

Authors:  Víctor R De Jesús; Joanne V Mei; Suzanne K Cordovado; Carla D Cuthbert
Journal:  Int J Neonatal Screen       Date:  2015

3.  Arginase 1 Deficiency: using genetic databases as a tool to establish global prevalence.

Authors:  C Catsburg; S Anderson; N Upadhyaya; M Bechter
Journal:  Orphanet J Rare Dis       Date:  2022-03-02       Impact factor: 4.123

4.  Argininemia as a cause of severe chronic stunting in a low-resource developing country setting: a case report.

Authors:  Nora King; Romina Alvizures; Pablo García; Ann Wessel; Peter Rohloff
Journal:  BMC Pediatr       Date:  2016-08-22       Impact factor: 2.125

5.  Harmonizing Newborn Screening Laboratory Proficiency Test Results Using the CDC NSQAP Reference Materials.

Authors:  Charles Austin Pickens; Maya Sternberg; Mary Seeterlin; Víctor R De Jesús; Mark Morrissey; Adrienne Manning; Sonal Bhakta; Patrice K Held; Joanne Mei; Carla Cuthbert; Konstantinos Petritis
Journal:  Int J Neonatal Screen       Date:  2020-09-17
  5 in total

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