Skip to main content
Canadian Medical Association Journal logoLink to Canadian Medical Association Journal
. 1964 Jun 6;90(23):1312–1315.

Case-Finding in Phenylketonuria

I. Report of a Survey By the College of General Practice of Canada

M W Partington, R M Anderson
PMCID: PMC1927188  PMID: 14155126

Abstract

In the years 1961 and 1962 the College of General Practice of Canada undertook a survey to detect infants with phenylketonuria. Routine urine tests for phenylketonuria were performed on all babies in a number of practices and records were kept. On a total of 4334 babies 6247 tests were carried out. Physicians' comments and the ages at which first, second and third urine tests were performed are reported. In an 18-month period, three confirmed and two probable cases of phenylketonuria were discovered.

Although it is not necessarily the most efficient method of case-finding, it is recommended that testing the urine for phenylketonuria should be a part of routine baby care.

Full text

PDF
1312

Images in this article

Selected References

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

  1. ARMSTRONG M. D., LOW N. L. Phenylketonuria VIII. Relation between age, serum phenylalanine level, and phenylpyruvic acid excretion. Proc Soc Exp Biol Med. 1957 Jan;94(1):142–146. doi: 10.3181/00379727-94-22880. [DOI] [PubMed] [Google Scholar]
  2. BERRY H. K., SUTHERLAND B. S., GUEST G. M. Cincinnati phenylketonuria detection program--a progress note. JAMA. 1961 Nov 25;178:842–842. doi: 10.1001/jama.1961.73040470020015. [DOI] [PubMed] [Google Scholar]
  3. CENTERWALL W. R., CENTERWALL S. A., ARMON V., MANN L. B. Phenylketonuria. II. Results of treatment of infants and young children. A report of 10 cases. J Pediatr. 1961 Jul;59:102–118. doi: 10.1016/s0022-3476(61)80217-5. [DOI] [PubMed] [Google Scholar]
  4. CENTERWALL W. R., CHINNOCK R. F., PUSAVAT A. Phenylketonuria: screening programs and testing methods. Am J Public Health Nations Health. 1960 Nov;50:1667–1677. doi: 10.2105/ajph.50.11.1667. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. FARQUHAR J. W., KANSAS E. T., TAIT H. P. Problems of routine screening for phenylketonuria. Lancet. 1962 Sep 8;2(7254):498–500. doi: 10.1016/s0140-6736(62)90358-6. [DOI] [PubMed] [Google Scholar]
  6. GIBBS N. K., WOOLF L. I. Tests for phenylketonuria: results of a one-year programme for its detection in infancy and among mental defectives. Br Med J. 1959 Sep 26;2(5151):532–535. doi: 10.1136/bmj.2.5151.532. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. GUTHRIE R., SUSI A. A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS. Pediatrics. 1963 Sep;32:338–343. [PubMed] [Google Scholar]
  8. PARTINGTON M. W., LEWIS E. J. Variations with age in plasma phenylalanine and tyrosine levels in phenylketonuria. J Pediatr. 1963 Mar;62:348–357. doi: 10.1016/s0022-3476(63)80131-6. [DOI] [PubMed] [Google Scholar]
  9. PARTINGTON M. W. Observations on phenylketonuria in Ontario. Can Med Assoc J. 1961 May 6;84:985–991. [PMC free article] [PubMed] [Google Scholar]
  10. PARTINGTON M. W. Variations in intelligence in phenylktonuria. Can Med Assoc J. 1962 Apr 21;86:736–743. [PMC free article] [PubMed] [Google Scholar]

Articles from Canadian Medical Association Journal are provided here courtesy of Canadian Medical Association

RESOURCES