Literature DB >> 6787336

Diet termination in children with phenylketonuria: a review of psychological assessments used to determine outcome.

S E Waisbren, R R Schnell, H L Levy.   

Abstract

This paper reviews the 19 published studies that have utilized psychological assessments in determining the outcome of children with phenylketonuria who have discontinued a phenylalanine-restricted diet. About half the studies showed that, after diet termination, the intellectual performance of children decreased, while the other studies indicated that the intellectual performance of the children did not change. Difficulties in the use of intelligence tests to answer questions about diet termination are outlined. Due to the methodological difficulties and the varying results reported, the issue concerning the safety of diet discontinuation remains unresolved. The conclusion is that the task now is to differentiate those children who should remain on the diet from those who may safely terminate.

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Year:  1980        PMID: 6787336     DOI: 10.1007/BF02312549

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  29 in total

1.  TERMINATION OF DIETARY TREATMENT FOR PHENYLKETONURIA.

Authors:  P R VANDEMAN
Journal:  Am J Dis Child       Date:  1963-11

2.  Termination of dietary treatment of phenylketonuria.

Authors:  F A HORNER; C W STREAMER; L L ALEJANDRINO; L H REED; F IBBOTT
Journal:  N Engl J Med       Date:  1962-01-11       Impact factor: 91.245

3.  Effect of stopping the low phenylalanine diet on the intellectual progress of children with phenylketonuria.

Authors:  I Smith; M Lobascher; J Stevenson; O H Wolff
Journal:  Ann Clin Biochem       Date:  1977-05       Impact factor: 2.057

4.  Phenylketonuria: mental development, behavior, and termination of low phenylalanine diet.

Authors:  I M Hackney; W B Hanley; W Davidson; L Lindsao
Journal:  J Pediatr       Date:  1968-05       Impact factor: 4.406

5.  Controlled observations of phenylketonuric children on and during withdrawal from low phenylalanine diet.

Authors:  O H Wolff
Journal:  Arch Dis Child       Date:  1968-12       Impact factor: 3.791

6.  Termination of dietary treatment of phenylketonuria.

Authors:  D Murphy
Journal:  Ir J Med Sci       Date:  1969-04       Impact factor: 1.568

7.  Treated phenylketonuria: intelligence and blood phenylalanine levels.

Authors:  R Fuller; J Shuman
Journal:  Am J Ment Defic       Date:  1971-03

8.  Discontinuing the phenylalamine-restricted diet in young children with PKY. Psychosocial aspects.

Authors:  S M Pueschel; S Yeatman; C Hum
Journal:  J Am Diet Assoc       Date:  1977-05

9.  Evaluation of the effects of terminating the diet in phenylketonuria.

Authors:  G Solomons; L Keleske; E Opitz
Journal:  J Pediatr       Date:  1966-10       Impact factor: 4.406

10.  Neurological disturbance in a phenylketonic child after discontinuation of dietary treatment.

Authors:  B Wood
Journal:  Dev Med Child Neurol       Date:  1976-10       Impact factor: 5.449

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  19 in total

1.  Disturbed myelination in patients with treated hyperphenylalaninaemia: evaluation with magnetic resonance imaging.

Authors:  U Bick; G Fahrendorf; A C Ludolph; P Vassallo; J Weglage; K Ullrich
Journal:  Eur J Pediatr       Date:  1991-01       Impact factor: 3.183

2.  Effect of genotype on changes in intelligence quotient after dietary relaxation in phenylketonuria and hyperphenylalaninaemia.

Authors:  L G Greeves; C C Patterson; D J Carson; R Thom; M C Wolfenden; J Zschocke; C A Graham; N C Nevin; E R Trimble
Journal:  Arch Dis Child       Date:  2000-03       Impact factor: 3.791

3.  The influence of blood phenylalanine levels on neurocognitive function in adult PKU patients.

Authors:  A Bartus; F Palasti; E Juhasz; E Kiss; E Simonova; Cs Sumanszki; P Reismann
Journal:  Metab Brain Dis       Date:  2018-06-12       Impact factor: 3.584

4.  Increased neurotransmitter biosynthesis in phenylketonuria induced by phenylalanine restriction or by supplementation of unrestricted diet with large amounts of tyrosine.

Authors:  C Lykkelund; J B Nielsen; H C Lou; V Rasmussen; A M Gerdes; E Christensen; F Güttler
Journal:  Eur J Pediatr       Date:  1988-12       Impact factor: 3.183

5.  The effects of diet discontinuation in children with phenylketonuria.

Authors:  R Koch; C G Azen; N Hurst; E G Friedman; K Fishler
Journal:  Eur J Pediatr       Date:  1987       Impact factor: 3.183

6.  Long-term follow up of patients with classical phenylketonuria after diet relaxation at 5 years of age. The Paris Study.

Authors:  F Rey; V Abadie; F Plainguet; J Rey
Journal:  Eur J Pediatr       Date:  1996-07       Impact factor: 3.183

7.  Intellectual development of the patients of the German Collaborative Study of children treated for phenylketonuria.

Authors:  P Burgard; E Schmidt; A Rupp; W Schneider; H J Bremer
Journal:  Eur J Pediatr       Date:  1996-07       Impact factor: 3.183

8.  Intelligence and professional career in young adults treated early for phenylketonuria.

Authors:  H Schmidt; P Burgard; J Pietz; A Rupp
Journal:  Eur J Pediatr       Date:  1996-07       Impact factor: 3.183

9.  Diet policies of PKU clinics in the United States.

Authors:  V E Schuett; E S Brown
Journal:  Am J Public Health       Date:  1984-05       Impact factor: 9.308

10.  Adults with untreated phenylketonuria: out of sight, out of mind.

Authors:  Glynis H Murphy; Sally M Johnson; Allayne Amos; Eleanor Weetch; Rosemary Hoskin; Brian Fitzgerald; Maggie Lilburn; Lesley Robertson; Philip Lee
Journal:  Br J Psychiatry       Date:  2008-12       Impact factor: 9.319

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