Literature DB >> 21648281

Thyroid dysfunctions in children detected in mass screening for congenital hypothyroidism.

Malgorzata Kumorowicz-Czoch1, Dorota Tylek-Lemanska, Jerzy Starzyk.   

Abstract

BACKGROUND: Congenital hypothyroidism (CH) affects approximately 1:3000-1:4000 infants.
OBJECTIVES: To determine the prevalence of CH and isolated hyperthyrotropinemia (IHT) in newborns selected in mass screening for CH.
METHODS: Mass screening of 233,120 neonates born in southeastern Poland was carried out and CH-suspected children were identified. Serum thyroid-stimulating hormone and free thyroxine levels were determined during first confirmation and diagnosis re-evaluation in 118 and 34 children, respectively. Additionally, the patients were subjected to thyroid ultrasonography (n=53) and/or scintiscan (n=28).
RESULTS: Out of 118 children, first confirmation indicated CH in 58 neonates and IHT in 4 neonates. Out of these, 34 were re-evaluated with regard to diagnosis. A final diagnosis of permanent CH was reported in 34 children with thyroid dysgenesis (n=27) or dyshormonogenesis (n=7), transient CH affected 15 children, and permanent IHT was diagnosed in 6 children. CH prevalence was 1:4570 (permanent 1:6475, transient 1:38,853) and permanent IHT 1:38,853.
CONCLUSIONS: The prevalence of CH and IHT corresponds to the prevalence of the condition in iodine-sufficient and borderline iodine-deficient areas.

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Year:  2011        PMID: 21648281     DOI: 10.1515/jpem.2011.080

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


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