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DC Field | Value | Language |
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dc.date.accessioned | 2022-10-06T06:05:28Z | - |
dc.date.available | 2022-10-06T06:05:28Z | - |
dc.date.issued | 2007-02 | - |
dc.identifier.citation | Sağlam, H. vd. (2007). "Increased incidence of congenital hypothyroidism due to iodine deficiency". Pediatrics International, 49(1), 76-79. | en_US |
dc.identifier.issn | 1442-200X | - |
dc.identifier.issn | 1328-8067 | - |
dc.identifier.uri | https://doi.org/10.1111/j.1442-200X.2007.02297.x | - |
dc.identifier.uri | https://onlinelibrary.wiley.com/doi/10.1111/j.1442-200X.2007.02297.x | - |
dc.identifier.uri | http://hdl.handle.net/11452/28982 | - |
dc.description.abstract | Background: The incidence of congenital hypothyroidism (CH) is expected to be elevated in iodine-deficient areas. In this study, the authors aimed to determine the incidence of transient and permanent CH in a large city which is known to be in the zone of moderate iodine deficiency. Methods:Newborn babies in Bursa, Turkey, were screened by measurement of serum thyroid-stimulating hormone (TSH) obtained by heel prick. The babies who had a serum TSH > 20 mIU/L were recalled for measurement of T4 and TSH in venous serum. Results:A total of 11 770 newborns were screened over a period of 9 years. The incidence of CH was found to be 1/840. However, after excluding the transient cases, permanent CH was diagnosed in 1/2354. It was impossible to distinguish transient patients from permanent CH by initial laboratory tests (P > 0.05). The estimated power of the study in determining the incidence of CH in the population was 90% (P < 0.05). Conclusions:The authors conclude that the incidence of CH is very high in their population which warrants a country-wide neonatal screening program. Since transient cases cannot be distinguished and untreated transient hypothyroidism may also cause mental retardation, treatment must be started as early as possible with frequent monitoring to optimize the outcome and identify the transient patients. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Congenital | en_US |
dc.subject | Hypothyroidism | en_US |
dc.subject | Incidence | en_US |
dc.subject | Iodine | en_US |
dc.subject | Screening | en_US |
dc.subject | Disorders | en_US |
dc.subject | World | en_US |
dc.subject.mesh | Incidence | en_US |
dc.subject.mesh | Congenital hypothyroidism | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Infant, newborn | en_US |
dc.subject.mesh | Lodine | en_US |
dc.subject.mesh | Thyrotropin | en_US |
dc.subject.mesh | Thyroxine | en_US |
dc.subject.mesh | Turkey | en_US |
dc.title | Increased incidence of congenital hypothyroidism due to iodine deficiency | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000243637000015 | tr_TR |
dc.identifier.scopus | 2-s2.0-33846445272 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Farmakoloji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Biyoistatistik Anabilim Dalı. | tr_TR |
dc.contributor.orcid | 0000-0003-0710-5422 | tr_TR |
dc.contributor.orcid | 0000-0002-2382-290X | tr_TR |
dc.identifier.startpage | 76 | tr_TR |
dc.identifier.endpage | 79 | tr_TR |
dc.identifier.volume | 49 | tr_TR |
dc.identifier.issue | 1 | tr_TR |
dc.relation.journal | Pediatrics International | en_US |
dc.contributor.buuauthor | Sağlam, Halil | - |
dc.contributor.buuauthor | Büyükuysal, Levent | - |
dc.contributor.buuauthor | Köksal, Nilgün | - |
dc.contributor.buuauthor | Ercan, İlker | - |
dc.contributor.researcherid | C-7392-2019 | tr_TR |
dc.contributor.researcherid | AAG-8393-2021 | tr_TR |
dc.identifier.pubmed | 17250510 | tr_TR |
dc.subject.wos | Pediatrics | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q4 | en_US |
dc.contributor.scopusid | 35612700100 | tr_TR |
dc.contributor.scopusid | 6507171811 | tr_TR |
dc.contributor.scopusid | 7003323615 | tr_TR |
dc.contributor.scopusid | 6603789069 | tr_TR |
dc.contributor.scopusid | 6701427186 | tr_TR |
dc.subject.scopus | Congenital Hypothyroidism; Thyroid Dysgenesis; Newborn Screening | en_US |
dc.subject.emtree | Laboratory test | en_US |
dc.subject.emtree | Thyrotropin | en_US |
dc.subject.emtree | Thyroxine | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Clinical article | en_US |
dc.subject.emtree | Congenital hypothyroidism | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Drug withdrawal | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Lodine deficiency | en_US |
dc.subject.emtree | Newborn | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Mental deficiency | en_US |
dc.subject.emtree | Morbidity | en_US |
dc.subject.emtree | Population | en_US |
dc.subject.emtree | Priority journal | en_US |
dc.subject.emtree | Newborn screening | en_US |
dc.subject.emtree | Prick test | en_US |
dc.subject.emtree | Screening test | en_US |
dc.subject.emtree | Thyrotropin blood level | en_US |
dc.subject.emtree | Turkey (republic) | en_US |
Appears in Collections: | PubMed Scopus Web of Science |
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