Diet discontinuation in phenylketonuria

The Collaborative Study of Children Treated for phenylketonuria (PKU) is being conducted in 15 medical centers throughout the United States.1 In this study, initiated in 1967, 140 PKU children were treated from near birth to 6 years of age. At age 6, with the consent of the parents, each child was r...

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Veröffentlicht in:	Pediatrics (Evanston) 1979-05, Vol.63 (5), p.823-824
Hauptverfasser:	Williamson, M, Koch, R, Berlow, S
Format:	Artikel
Sprache:	eng
Schlagworte:	Child Humans Intellectual Disability - etiology Intelligence Phenylketonurias - diet therapy Phenylketonurias - psychology
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description	The Collaborative Study of Children Treated for phenylketonuria (PKU) is being conducted in 15 medical centers throughout the United States.1 In this study, initiated in 1967, 140 PKU children were treated from near birth to 6 years of age. At age 6, with the consent of the parents, each child was randomly assigned to one of two groups, either to continue on a phenylalanine-restricted diet, or to discontinue dietary restrictions and eat a normal diet.
doi_str_mv	10.1542/peds.63.5.823a
format	Article
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source	MEDLINE; EZB-FREE-00999 freely available EZB journals
subjects	Child Humans Intellectual Disability - etiology Intelligence Phenylketonurias - diet therapy Phenylketonurias - psychology
title	Diet discontinuation in phenylketonuria
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