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High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients

Y. Özer,A. Anık, U. Sayılı, U. Tercan, R. Deveci Sevim, S. Güneş, M. Buhur Pirimoğlu, S. Elmaoğulları, İ. Dündar, D. Ökdemir,Ö. Besci, A. Jalilova, D. Çiçek, B. Singin, Ş. E. Ulu,H. Turan, S. Albayrak, Z. Kocabey Sütçü, B. S. Eklioğlu, E. Eren,S. Çetinkaya, Ş. Savaş-Erdeve, İ. Esen,K. Demir,Ş. Darcan,N. Hatipoğlu, M. Parlak,F. Dursun,Z. Şıklar,M. Berberoğlu,M. Keskin,Z. Orbak,B. Tezel, E. Yürüker,B. Keskinkılıç, F. Kara,E. Erginöz,F. Darendeliler,O. Evliyaoğlu

Journal of Endocrinological Investigation(2024)

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Abstract
We aimed to determine the frequency of transient congenital hypothyroidism (TCH) in 17 participating centers in Türkiye, evaluate the etiological distribution in permanent congenital hypothyroidism (PCH) cases, and investigate the role of laboratory and clinical findings in predicting TCH. This retrospective observational multicenter study included patients from 17 pediatric endocrinology centers identified by “National Newborn Screening Program” (NNSP) who were born in 2015 and followed for 6 years. Demographic, clinical, and laboratory information of the cases were compiled through the database http://cedd.saglik-network.org (CEDD-NET). Of the 239 cases initially treated for CH, 128 (53.6
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Key words
Neonatal screening,Transient congenital hypothyroidism,Permanent congenital hypothyroidism,Frequency,Etiology,Thyroxine
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