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Archives of Disease in Childhood logoLink to Archives of Disease in Childhood
. 1975 Apr;50(4):264–268. doi: 10.1136/adc.50.4.264

Screening for inherited metabolic disease in Wales using urine-impregnated filter paper.

D M Bradley
PMCID: PMC1544450  PMID: 1147666

Abstract

Urine specimens from 135 295 infants have been collected on filter papers and tested for 7 abnormal urinary constituents using spot tests and paper chromatography. The method has detected 5 infants with phenylketonuria, 4 with histidinaemia, 5 with cystinuria, 5 with diabetes mellitus, and one with alcaptonuria. Transient abnormalities such as tyrosyluria, generalized aminoaciduria, cystinuria, and glycosuria have been noted. 2 phenylketonuric infants failed to excrete a detectable quantity of o-hydroxyphenlacetic acid at the time of testing. The findings show that the detection of this compound in urine is an unreliable method of screening for phenylketonuria.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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