Literature DB >> 7064926

Screening for metabolic disease in a metropolitan hospital.

I Krieger, M Nigro, Q Taqi.   

Abstract

Screening for metabolic diseases at Children's Hospital of Michigan, Detroit during 1978 and 1979 led to the discovery of 7.5 cases per year, representing a marked increase over previous years. Five cases of organic aciduria were identified during this two-year period by use of urinary gas chromatography. Four of these were found to have methylmalonic aciduria. The increase in detection rate was due to the addition of an organic acid screening technique and greater use of two standard screening tests. The yield of screening by these two tests also improved, which we attribute to the better use of specific criteria. Inclusion of a simple urine screening test for methylmalonic acid is recommended in the workup of infants with episodic vomiting, lethargy, acidosis, or catastrophic illness.

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Year:  1982        PMID: 7064926     DOI: 10.1001/archpedi.1982.03970380037009

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  2 in total

1.  Inherited metabolic disorders in Turkey.

Authors:  I Ozalp; T Coskun; S Tokol; G Demircin; E Mönch
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

Review 2.  Clinical biochemistry of the neonatal period: immaturity, hypoxia, and metabolic disease.

Authors:  R A Harkness
Journal:  J Clin Pathol       Date:  1987-09       Impact factor: 3.411

  2 in total

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