Phenylketonuria in Adolescents and Adult Persons in Slovakia
Fenylketonúria adolescentov a dospelých na Slovensku
Autori predkladajú analýzu súboru pacientov s fenylketonúriou v adolescentom veku a dospelosti v Centre prediagnostiku a liečbu hyperfenylalaninémie v Bratislave.V rámci sledovania sa zamerali na celkový počet pacientov,priemerný vek, rozdelenie podľa pohlavia a veku, frekvenciu kontrol a návštev, analýzu neskorého záchytuochorenia, vzdelania podľa vekových skupín, na liečbu pacientov, typ liečby a výsledky psychologického sledovania.
Klíčová slova:
hyperfenylalaninémia, fenylketonúria adolescentov a dospelých
Authors:
O. Ürge 1; J. Strnová 2; B. Mosendzová 1
Authors‘ workplace:
Klinika laboratórnej medicíny, FNsP akademika L. Dérera, Bratislava1 prednosta prof. MUDr. RNDr. G. Kováč, CSc., MBA Klinika pre deti a dorast A. Getlíka, SZU, NsP sv. Cyrila a Metoda, Bratislava2 prednostka doc. MUDr. K. Furková, CSc.
Published in:
Čes-slov Pediat 2003; (7): 423-425.
Category:
Overview
The authors present an analysis of a cohort of patients suffering from phenylketonuria during adolescence andat the adult age having been treated in the Center for diagnosis and therapy of hyperphenylalaninemia located inBratislava. Within the framework of the observation the authors paid attention to the number of patients, meanage, distribution according to sex and age, the frequency of control examinations and visits, analysis of the latediagnosis of the disease, education in relation to the age groups, therapy of the patients, type of treatment and theresults of psychological examination.
Key words:
hyperphenylalaninemia, phenylketonuria in adolescents and adult individuals
Labels
Neonatology Paediatrics General practitioner for children and adolescentsArticle was published in
Czech-Slovak Pediatrics
2003 Issue 7
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All articles in this issue
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- 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
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