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[Phenylketonuria: illness experience and coping mechanisms].

作者信息

Weglage J, Fünders B, von Teeffelen-Heithoff A, Ullrich K

机构信息

Universitätskinderklinik Münster.

出版信息

Z Kinder Jugendpsychiatr. 1993 Sep;21(3):156-62.

PMID:8237123
Abstract

If patients with PKU follow a strict diet low in phenylalanine from soon after birth their intellectual and psychomotor development will be within the normal range. Recent studies have shown that it is necessary to continue the burdensome diet throughout one's life. This is in contrast to past practice and puts additional emphasis on psychosocial aspects of PKU. In the present retrospective study we investigated how adolescent patients and their relatives' experience and cope with this chronic disease.

摘要

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[Phenylketonuria: illness experience and coping mechanisms].
Z Kinder Jugendpsychiatr. 1993 Sep;21(3):156-62.
2
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引用本文的文献

1
The truth of treating patients with phenylketonuria after childhood: the need for a new guideline.儿童期后苯丙酮尿症患者的治疗现状:制定新指南的必要性
J Inherit Metab Dis. 2008 Dec;31(6):673-9. doi: 10.1007/s10545-008-0918-6. Epub 2008 Aug 12.
2
Intellectual and school performance in adolescents with phenylketonuria according to their dietary compliance. The Czech-Slovak Collaborative Study.
Eur J Pediatr. 1996 Jul;155 Suppl 1:S56-8. doi: 10.1007/pl00014251.