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Archives of Disease in Childhood 1979;54:593-598; doi:10.1136/adc.54.8.593
Copyright © 1979 BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health

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Changing incidence of neonatal hypermethioninaemia: implications for the detection of homocystinuria.

P D Whiteman, B E Clayton, R S Ersser, P Lilly, J W Seakins

The Guthrie test was used to measure blood methionine concentrations in 670 764 neonates during the period from May 1970 to December 1977. Raised values (greater than 4 mg/100 ml; 268 mumol/l) were found in 147 babies (6--14 days old) and 55 of these still had raised values when retested 2--6 weeks later. 48 infants had transient hypermethioninaemia of at least 3 weeks' duration, one had a more persistent form associated with abnormal liver function tests, 3 had different forms of homocystinuria, and one infant, who was asymptomatic at the time of detection, had hypermethioninaemia associated with a rapidly fatal form of tyrosinamiea (tyrosinosis). Two infants could not be followed up. Transient hypermethioninaemia has not been detected in this laboratory since 1975. There was a greatly reduced incidence of transient hypermethioninaemia in girls after 1972 and in boys after 1975; this may have been due to recent changes in infant practices in the UK. Homocystinuria was last detected in this laboratory in 1972; the apparent change in incidence is significant (P less than 0.05) and suggests that the diagnostic value of this screening procedure should be reassessed.





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M. J. Peterschmitt, J. R. Simmons, and H. L. Levy
Reduction of False Negative Results in Screening of Newborns for Homocystinuria
N. Engl. J. Med., November 18, 1999; 341(21): 1572 - 1576.
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D. M Isherwood
Homocystinuria
BMJ, October 26, 1996; 313(7064): 1025 - 1026.
[Full Text]




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