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Newborn screening in southeastern Europe

Authors :
Groselj, Urh
Zerjav Tansek, Mojca
Smon, Andraz
Angelkova, Natalija
Anton, Dana
Barić, Ivo
Đorđević, Maja
Grimci, Lindita
Ivanova, Maria
Kadam, Adil
Kotori, Vjosa Mulliqi
Maksić, Hajrija
Marginean, Oana
Margineanu, Otilia
Milijanović, Olivera
Moldovanu, Florentina
Muresan, Mariana
Murko, Simona
Nanu, Michaela
Lampret, Barbka Repic
Samardzić, Mira
Sarnavka, Vladimir
Savov, Aleksei
Stojiljković, Maja
Suzić, Biljana
Tincheva, Radka
Tahirović, Husref
Toromanović, Alma
Usurelu, Natalia
Battelino, Tadej
Groselj, Urh
Zerjav Tansek, Mojca
Smon, Andraz
Angelkova, Natalija
Anton, Dana
Barić, Ivo
Đorđević, Maja
Grimci, Lindita
Ivanova, Maria
Kadam, Adil
Kotori, Vjosa Mulliqi
Maksić, Hajrija
Marginean, Oana
Margineanu, Otilia
Milijanović, Olivera
Moldovanu, Florentina
Muresan, Mariana
Murko, Simona
Nanu, Michaela
Lampret, Barbka Repic
Samardzić, Mira
Sarnavka, Vladimir
Savov, Aleksei
Stojiljković, Maja
Suzić, Biljana
Tincheva, Radka
Tahirović, Husref
Toromanović, Alma
Usurelu, Natalia
Battelino, Tadej
Source :
Molecular Genetics and Metabolism
Publication Year :
2014

Abstract

The aim of our study was to assess the current state of newborn screening (NBS) in the region of southeastern Europe, as an example of a developing region, focusing also on future plans. Responses were obtained from 11 countries. Phenylketonuria screening was not introduced in four of 11 countries, while congenital hypothyroidism screening was not introduced in three of them; extended NBS programs were non-existent. The primary challenges were identified. Implementation of NBS to developing countries worldwide should be considered as a priority.

Details

Database :
OAIster
Journal :
Molecular Genetics and Metabolism
Notes :
Molecular Genetics and Metabolism
Publication Type :
Electronic Resource
Accession number :
edsoai.on1368248506
Document Type :
Electronic Resource