-
Medical journals
- Career
Aspects of Psychological Care of Patients with Phenylketonuria
Authors: L. Vaďurová 1; S. Šťastná 1; J. Hyánek 1,2
Authors‘ workplace: Ústav dědičných metabolických poruch VFN a 1. LF UK, Praha1 přednosta prof. MUDr. M. Elleder, DrSc. Oddělení klinické biochemie, hematologie a imunologie, Nemocnice Na Homolce, Praha2 primář prof. MUDr. J. Hyánek, DrSc.
Published in: Čes-slov Pediat 2003; (7): 441-446.
Category:
Overview
Psychological care is the necessary part of complex lifetime care of patients with phenylketonuria/hyperphenylalaninemia(PKU/HPA). The aim of the article is to summarize long-time experience of the clinical psychologistwith care of the group of 14 women with PKU/HPA in the critical periods of their life, with emphasis on the periodof preconception care and pregnancy. Superior psychological care improves dietary compliance of patients withPKU/HPA and reduces risk of phenylalanine embryopathy or fetopathy in embryo and fetus.
Key words:
phenylketonuria, hyperphenylalaninemia, psychology, anxiety, compliance
Labels
Neonatology Paediatrics General practitioner for children and adolescents
Article was published inCzech-Slovak Pediatrics
2003 Issue 7-
All articles in this issue
- Organization of the Care of Patients with Hyperphenylalaninemia in Slovakia
- Methodic Guide to Diagnostics of Congenital Disorders of Glycosylation (CDG)
- Phenylketonuria in Adolescents and Adult Persons in Slovakia
- MCAD Deficiency - Our Experience with Four Symptomatic Patients
- Selective Screening of Children at Risk of Early Atherosclerosis in the Czech Republic
- Glycogenosis Type II - Infantile Form (Morbus Pompe) in the Czech and Slovak Population
- Aspects of Psychological Care of Patients with Phenylketonuria
- Unusual Cause of Severe Lactate Acidosis in a Seven-month Child
- Analysis of Consequences of Phenylketonuria in Relation to Metabolic Compensation and Age
- Clinical and Molecular Analyses in Eight Children with Congenital Disorders of Glycosylation
- Megaloblastic Anemia 1 (Imerslund-Gräsbeck)
- Tandem Mass Spectrometry - The Future of Newborn Screening of Inborn Errors of Metabolism
- Czech-Slovak Pediatrics
- Journal archive
- Current issue
- Online only
- About the journal
Most read in this issue- MCAD Deficiency - Our Experience with Four Symptomatic Patients
- Megaloblastic Anemia 1 (Imerslund-Gräsbeck)
- Tandem Mass Spectrometry - The Future of Newborn Screening of Inborn Errors of Metabolism
- Clinical and Molecular Analyses in Eight Children with Congenital Disorders of Glycosylation
Login#ADS_BOTTOM_SCRIPTS#Forgotten passwordEnter the email address that you registered with. We will send you instructions on how to set a new password.
- Career