Literature DB >> 9575455

Development of the phenylketonuria screening programme in Estonia.

K Ounap1, H Lilleväli, A Metspalu, M Lipping-Sitska.   

Abstract

OBJECTIVE: To develop the phenylketonuria (PKU) screening programme in Estonia.
METHOD: All data about patients with PKU, born during 1980-92, were documented to establish its prevalence at birth in Estonia. Newborn screening for the diagnosis and treatment of PKU was started in Estonia in 1993 and the prevalence at birth established by screening. Phenylalanine was determined from filter paper blood by a modified fluorometric method based on enhancement of the fluorescence of a phenylalanine-ninhydrin reaction product by L-leucyl-L-alanine.
RESULTS: During three years (1993-5) 36,074 newborns (85% of the total) were screened for PKU. PKU was diagnosed in six cases during the first four to six weeks of life. All investigated cases could be classified as classical PKU. No cases of mild forms of hyperphenylalaninaemia were diagnosed. The retrospective study showed an average incidence of PKU of 1 in 8090, the prospective study identified a comparable incidence of 1 in 6010 live births.
CONCLUSION: The prevalence at birth of classic PKU in Estonia is higher than the average in Europe and similar to that of some eastern and middle European countries.

Entities:  

Mesh:

Year:  1998        PMID: 9575455     DOI: 10.1136/jms.5.1.22

Source DB:  PubMed          Journal:  J Med Screen        ISSN: 0969-1413            Impact factor:   2.136


  7 in total

1.  Hyperphenylalaninaemias in Estonia: Genotype-Phenotype Correlation and Comparative Overview of the Patient Cohort Before and After Nation-Wide Neonatal Screening.

Authors:  Hardo Lilleväli; Karit Reinson; Kai Muru; Kristi Simenson; Ülle Murumets; Tõnu Möls; Katrin Õunap
Journal:  JIMD Rep       Date:  2017-09-28

2.  The live-birth prevalence of mucopolysaccharidoses in Estonia.

Authors:  Külliki Krabbi; Kairit Joost; Riina Zordania; Inga Talvik; Reet Rein; Jan G M Huijmans; Frans V Verheijen; Katrin Õunap
Journal:  Genet Test Mol Biomarkers       Date:  2012-04-05

3.  Birth prevalence of phenylalanine hydroxylase deficiency: a systematic literature review and meta-analysis.

Authors:  Pamela K Foreman; Andrea V Margulis; Kimberly Alexander; Renee Shediac; Brian Calingaert; Abenah Harding; Manel Pladevall-Vila; Sarah Landis
Journal:  Orphanet J Rare Dis       Date:  2021-06-03       Impact factor: 4.123

4.  Genetics in an isolated population like Finland: a different basis for genomic medicine?

Authors:  Helena Kääriäinen; Juha Muilu; Markus Perola; Kati Kristiansson
Journal:  J Community Genet       Date:  2017-07-20

5.  FLAD1-associated multiple acyl-CoA dehydrogenase deficiency identified by newborn screening.

Authors:  Kai Muru; Karit Reinson; Kadi Künnapas; Hardo Lilleväli; Zahra Nochi; Signe Mosegaard; Sander Pajusalu; Rikke K J Olsen; Katrin Õunap
Journal:  Mol Genet Genomic Med       Date:  2019-08-08       Impact factor: 2.183

6.  Global prevalence of classic phenylketonuria based on Neonatal Screening Program Data: systematic review and meta-analysis.

Authors:  Hamid Reza Shoraka; Ali Akbar Haghdoost; Mohammad Reza Baneshi; Zohre Bagherinezhad; Farzaneh Zolala
Journal:  Clin Exp Pediatr       Date:  2020-02-06

Review 7.  Food Regime for Phenylketonuria: Presenting Complications and Possible Solutions.

Authors:  Sudipt Kumar Dalei; Nidhi Adlakha
Journal:  J Multidiscip Healthc       Date:  2022-01-18
  7 in total

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