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dc.contributor.authorGüran, Tülay
dc.contributor.authorTezel, Başak
dc.contributor.authorGürbüz, Fatih
dc.contributor.authorSelver Eklioğlu, Beray
dc.contributor.authorHatipoğlu, Nihal
dc.contributor.authorKara, Cengiz
dc.contributor.authorŞimşek, Enver
dc.contributor.authorÇizmecioğlu, Filiz Mine
dc.contributor.authorOzon, Alev
dc.contributor.authorBaş, Firdevs
dc.contributor.authorAydın, Murat
dc.contributor.authorDarendeliler, Feyza
dc.date.accessioned2021-06-02T10:39:53Z
dc.date.available2021-06-02T10:39:53Z
dc.date.issued2019
dc.identifier.issn1308-5727
dc.identifier.urihttp://dx.doi.org/10.4274/jcrpe.galenos.2018.2018.0117
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398187/
dc.identifier.urihttp://hdl.handle.net/11655/23833
dc.description.abstractObjective: Congenital adrenal hyperplasia (CAH) is the most common form of primary adrenal insufficiency in children. Neonatal screening for CAH is effective in detecting the salt-wasting (SW) form and in reducing mortality. In this study, our aim was to estimate the incidence of CAH in Turkey and to assess the characteristics and efficacy of the adopted newborn CAH screening strategy. Methods: A pilot newborn CAH screening study was carried out under the authority of the Turkish Directorate of Public Health. Newborn babies of ≥32 gestational weeks and ≥1500 gr birth weight from four cities, born between March 27-September 15, 2017 were included in the study. Screening protocol included one sample two-tier testing. In the first step, 17α-hydroxyprogesterone (17-OHP) was measured by fluoroimmunoassay in dried blood spots (DBS) obtained at 3-5 days of life. The cases with positive initial screening were tested by steroid profiling in DBS using a liquid chromatography-tandem mass spectrometry method to measure 17-OHP, 21-deoxycortisol (21-S), cortisol (F), 11-deoxycortisol and androstenedione as a second-tier test. The babies with a steroid ratio (21-S+17-OHP)/F of ≥0.5 were referred to pediatric endocrinology clinics for diagnostic assessment. Results: 38,935 infants were tested, 2265 (5.82%) required second-tier testing and 212 (0.54%) were referred for clinical assessment, six of whom were diagnosed with CAH (four males, two females). Four cases were identified as SW 21-hydroxylase deficiency (21-OHD) (two males, two females). One male baby had simple virilizing 21-OHD and one male baby had 11-OHD CAH. The incidence of classical 21-OHD in the screened population was 1:7,787. Conclusion: The incidence of CAH due to classical 21-OHD is higher in Turkey compared to previous reports. We, therefore, suggest that CAH be added to the newborn screening panel in Turkey. The use of steroid profiling as a second-tier test was found to improve the efficacy of the screening and reduce the number of false-positives.
dc.language.isoen
dc.relation.isversionof10.4274/jcrpe.galenos.2018.2018.0117
dc.rightsAttribution 4.0 United States
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleNeonatal Screening For Congenital Adrenal Hyperplasia In Turkey: A Pilot Study With 38,935 Infants
dc.title.alternativeNeonatal Screening for Congenital Adrenal Hyperplasia in Turkey
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalJournal Of Clinical Research In Pediatric Endocrinology
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları
dc.identifier.volume11
dc.identifier.issue1
dc.description.indexPubMed
dc.description.indexWoS
dc.description.indexScopus


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Attribution 4.0 United States
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