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Neonatal screening for congenital hypothyroidism in the Federation of Bosnia and Herzegovina: eight years' experience.

作者信息

Tahirović Husref, Toromanović Alma

机构信息

Department of Pediatrics, University Clinical Center, Trnovac bb, 75000 Tuzla, Bosnia and Herzegovina.

出版信息

Eur J Pediatr. 2009 May;168(5):629-31. doi: 10.1007/s00431-008-0801-3. Epub 2008 Jul 31.

DOI:10.1007/s00431-008-0801-3
PMID:18668261
Abstract

This report demonstrates the prevalence of primary congenital hypothyroidism (CH) in the Federation of Bosnia and Herzegovina and summarizes the laboratory data. Neonatal thyroid-stimulating hormone (TSH) was measured in whole blood drawn between the 3rd and 5th days of life and spotted on filter paper using the fluorometric assay. Among the 87,061 neonates, 22 had CH, 13 dysgenetic forms, and nine with thyroids in situ. No differences were found between the two types in terms of TSH and total T4 concentrations. However, thyroglobulin was significantly lower in patients with dysgenetic thyroid tissue (p=0.0023). We conclude that the prevalence of CH in the Federation of Bosnia and Herzegovina is 1:3,957 newborns.

摘要

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本文引用的文献

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Neonatal screening in Europe; the situation in 2004.欧洲的新生儿筛查;2004年的情况。
J Inherit Metab Dis. 2007 Aug;30(4):430-8. doi: 10.1007/s10545-007-0644-5. Epub 2007 Jul 6.
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High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis.甲状腺激素合成障碍患者中甲状腺过氧化物酶基因突变的高发生率。
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Neonatal thyroid disorders.新生儿甲状腺疾病
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Neonatal screening for congenital hypothyroidism: results and perspectives.新生儿先天性甲状腺功能减退症筛查:结果与展望。
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