Intelligence and quality of dietary treatment in phenylketonuria.

Archives of Disease in Childhood - Tập 65 Số 5 - Trang 472-478 - 1990
I Smith1, M G Beasley1, A. E. Ades1
1Department of Child Health, Institute of Child Health, London

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Two national surveys were conducted (in 1972 and 1980) to ensure that the register was complete. From the mid 1960s onwards a national programme of routine screening of urine for phenylketonuria between 3 and 6 weeks of age was progressively replaced by a system of blood testing between the 6th and 14th days'4; the change was virtually complete by 1971. For this reason we have distinguished between children born from 1964 to 1971 (cohort 1) and those born from 1972 to 1980 (cohort 2).

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