Literature DB >> 3939545

Successful adjustment to society by adults with phenylketonuria.

R Koch, M Yusin, K Fishler.   

Abstract

The study shows that most individuals between 16 and 25 years of age with PKU appear to function in a productive manner in society. Although they have not become professional men and women, they can acquire jobs of a skilled or semiskilled nature and perform them satisfactorily. The majority seemed content with their jobs and happy with the way their lives were progressing, although only 23% were financially independent. Of the patients interviewed, the majority had made friendships and appeared to keep them without much trouble. The majority of the patients would not tell their friends that they had PKU. The reason for this was that they felt uncomfortable acknowledging that they had this disorder.

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Year:  1985        PMID: 3939545     DOI: 10.1007/bf01805437

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


  6 in total

1.  Effect of a phenylalanine-restricted diet on patients with phenylketonuria; clinical observations in three cases.

Authors:  F A HORNER; C W STREAMER
Journal:  J Am Med Assoc       Date:  1956-08-25

2.  Intellectual performance of 36 phenylketonuria patients and their nonaffected siblings.

Authors:  J C Dobson; E Kushida; M Williamson; E G Friedman
Journal:  Pediatrics       Date:  1976-07       Impact factor: 7.124

3.  The incidence of Pku in Finland.

Authors:  J K Visakorpi; J Palo; O V Renkonen
Journal:  Acta Paediatr Scand       Date:  1971-11

4.  Correlates of intelligence test results in treated phenylketonuric children.

Authors:  M L Williamson; R Koch; C Azen; C Chang
Journal:  Pediatrics       Date:  1981-08       Impact factor: 7.124

5.  The frequency of PKU and hyperphenylalaninemia in Sweden - a study in institutions for the mentally retarded as well as in neonates.

Authors:  G Holmgren; A Larsson; H Palmstierna; J Alm
Journal:  Clin Genet       Date:  1976-12       Impact factor: 4.438

6.  Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria.

Authors:  S L Woo; A S Lidsky; F Güttler; T Chandra; K J Robson
Journal:  Nature       Date:  1983 Nov 10-16       Impact factor: 49.962

  6 in total
  7 in total

1.  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

2.  Group work with adolescent PKU girls and their mothers.

Authors:  B E Cohen; R Weiss; R Hadar; M Normand; S Shiloh; D Elhanati
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

3.  Adult psychosocial outcome in early-treated phenylketonuria.

Authors:  M D Ris; A M Weber; M M Hunt; H K Berry; S E Williams; N Leslie
Journal:  J Inherit Metab Dis       Date:  1997-08       Impact factor: 4.982

4.  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

5.  Agoraphobia in phenylketonuria.

Authors:  S E Waisbren; H L Levy
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

6.  Social outcome in treated individuals with inherited metabolic disorders: UK study.

Authors:  M Bhat; C Haase; P J Lee
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.750

7.  Evaluation of quality of life and description of the sociodemographic state in adolescent and young adult patients with phenylketonuria (PKU).

Authors:  Eva Simon; Martin Schwarz; Judith Roos; Nico Dragano; Max Geraedts; Johannes Siegrist; Gudrun Kamp; Udo Wendel
Journal:  Health Qual Life Outcomes       Date:  2008-03-26       Impact factor: 3.186

  7 in total

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