Organization of the Care of Patients with Hyperphenylalaninemia in Slovakia
Organizácia starostlivosti o pacientovs hyperfenylalaninémiou na Slovensku
Autori predkladajú organizáciu starostlivosti o pacientov s hyperfenylalaninémiou na Slovensku. V predloženejpráci je rozobratá metóda aktívneho vyhľadávania tejto dedičnej metabolickej poruchy od jeho započatia ažpo súčasnosť a zabezpečenie dlhodobej komplexnej starostlivosti o pacientov s hyperfenylalaninémiou.
Klíčová slova:
hyperfenylalaninémia, skríning, komplexná starostlivosť
Authors:
Strnová J.. Ürge O. 1 2; M. Beránková 1
Authors‘ workplace:
Klinika pre deti a dorast A. Getlíka, SZU, NsP sv. Cyrila a Metoda, Bratislava1 prednostka doc. MUDr. K. Furková, CSc. Klinika laboratórnej medicíny, FNsP akademika L. Dérera, Bratislava2 prednosta prof. MUDr. RNDr. G. Kováč, CSc., MBA
Published in:
Čes-slov Pediat 2003; (7): 421-422.
Category:
Overview
The authors describe organization of the care of patients suffering from hyperphenylalaninemia in Slovakia.The paper analyzes the method of active search for this hereditary metabolic disorder from the beginning to thepresent time and how the long-term complex care of the patients with hyperphenylalaninemia is provided.
Key words:
hyperphenylalaninemia, screening, complex care
Labels
Neonatology Paediatrics General practitioner for children and adolescentsArticle was published in
Czech-Slovak Pediatrics
2003 Issue 7
- The Importance of Limosilactobacillus reuteri in Administration to Diabetics with Gingivitis
- What Effect Can Be Expected from Limosilactobacillus reuteri in Mucositis and Peri-Implantitis?
-
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
- 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