Literature DB >> 66568

Phenylalanine metabolism and intellectual functioning among carriers of phenylketonuria and hyperphenylalaninaemia.

R C Ford, J L Berman.   

Abstract

All members of 63 families who had phenylketonuric or hyperphenylalaninaemic offspring received a phenylalanine tolerance test and an individual intelligence test. Parent carriers (heterozygotes, n=115) displayed a significant relationship (canonical correlation R=0.75, P is less than 0.05) between their ability to metabolise phenylalanine and their intellectual strengths and weaknesses. Mothers of hyperphenylalaniaemic children did not show this relationship. The number of carrier children (n=40) was too small for multivariate or sex analysis, but significant bivariate correlations were found for this group.

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Year:  1977        PMID: 66568     DOI: 10.1016/s0140-6736(77)92955-5

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  11 in total

1.  Neuropsychological deficits in obligatory heterozygotes for metachromatic leukodystrophy.

Authors:  H Kohn; P Manowitz; M Miller; A Kling
Journal:  Hum Genet       Date:  1988-05       Impact factor: 4.132

2.  Neuropsychological profile in parents of adult phenylketonuria patients.

Authors:  Gabriella Santangelo; Fausta Piscopo; Franco Santangelo; Luigi Trojano
Journal:  Neurol Sci       Date:  2017-11-09       Impact factor: 3.307

3.  Intracellular concentrations of phenylalanine, tyrosine and alpha-aminobutyric acid in 13 homozygotes and 19 heterozygotes for phenylketonuria compared with 26 normals.

Authors:  O Thalhammer; A Pollak; G Lubec; H Königshofer
Journal:  J Inherit Metab Dis       Date:  1981       Impact factor: 4.982

4.  Genes for super-intelligence?

Authors:  J A Sofaer; A E Emery
Journal:  J Med Genet       Date:  1981-12       Impact factor: 6.318

5.  Sex effect on the risk of mental retardation.

Authors:  S P Bessman
Journal:  Behav Genet       Date:  1980-05       Impact factor: 2.805

Review 6.  Inherited metabolic diseases affecting the carrier.

Authors:  W Endres
Journal:  J Inherit Metab Dis       Date:  1997-03       Impact factor: 4.982

7.  Neuropsychological and biochemical investigations in heterozygotes for phenylketonuria during ingestion of high dose aspartame (a sweetener containing phenylalanine).

Authors:  F Trefz; L de Sonneville; P Matthis; C Benninger; B Lanz-Englert; H Bickel
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

Review 8.  Diseases of phenylalanine metabolism.

Authors:  C E Parker
Journal:  West J Med       Date:  1979-10

9.  Diet, genetics, and mental retardation interaction between phenylketonuric heterozygous mother and fetus to produce nonspecific diminution of IQ: evidence in support of the justification hypothesis.

Authors:  S P Bessman; M L Williamson; R Koch
Journal:  Proc Natl Acad Sci U S A       Date:  1978-03       Impact factor: 11.205

10.  Intracellular phenylalanine and tyrosine concentrations in 19 heterozygotes for phenylketonuria (PKU) and 26 normals. Do the higher values in heterozygotes explain their lowered intellectual level?

Authors:  O Thalhammer; G Lubec; H Königshofer
Journal:  Hum Genet       Date:  1979-07-18       Impact factor: 4.132

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