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Research article summary (published 5 Sep 1974):

Natural history of phenylketonuria and influence of early treatment.

Full Abstract

This study describes the intellectual development of twenty-eight sibling pairs with phenylketonuria in which the index case presented because of retarded development. In twelve pairs (group I) the "second" sibling was born subsequently, and in sixteen (group II) there was a second sibling already in the family at the time of diagnosis of the index case. The intellectual outcome of the second siblings of group II suggests that approximately 1 in 6 or 7 patients with untreated classical phenylketonuria achieves an I.Q. above 70, although with evidence of intellectual impairment. The highly significant difference in intellectual outcome between the early treated second siblings of group I and the late or untreated second siblings of group II demonstrates the beneficial effect of early treatment on the intelligence of affected children.

 

Author information

Author/s: Smith, I (I); Wolff, O H (OH);

Journal and publication information

Publication Type: Journal Article

Journal: Lancet (Lancet), published in ENGLAND. (Language: eng)

Reference: 1974-Sep; vol 2 (issue 7880) : pp 540-4

Dates: Created 1975/03/10; Completed 1975/03/10; Revised 2004/11/17;

PMID: 4140266, status: MEDLINE (last retrieval date: 2/18/2009, IMS Date: )

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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MeSH headings (categories)

This article was linked to the MESH Headings shown below.

Associated Chemicals: Phenylacetates (0) ; Phenylpyruvic Acids (0) ; Phenylalanine (63-91-2)

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