Literature DB >> 28439194

Fetal neonatal hyperthyroidism: diagnostic and therapeutic approachment.

Selim Kurtoğlu1, Ahmet Özdemir1.   

Abstract

Fetal and neonatal hyperthyroidism may occur in mothers with Graves' disease. Fetal thyrotoxicosis manifestation is observed with the transition of TSH receptor stimulating antibodies to the fetus from the 17th-20th weeks of pregnancy and with the fetal TSH receptors becoming responsive after 20 weeks. The diagnosis is confirmed by fetal tachycardia, goiter and bone age advancement in pregnancy and maternal treatment is conducted in accordance. The probability of neonatal hyperthyroidism is high in the babies of mothers that have ongoing antithyroid requirement and higher antibody levels in the last months of pregnancy. Clinical manifestation may be delayed by 7-17 days because of the antithyroid drugs taken by the mother. Neonatal hyperthyroidism symptoms can be confused with sepsis and congenital viral infections. Herein, the diagnosis and therapeutic approach are reviewed in cases of fetal neonatal hyperthyroidism.

Entities:  

Keywords:  Fetal hyperthyroidism; Graves’ disease; neonatal hyperthyroidism; pregnancy

Year:  2017        PMID: 28439194      PMCID: PMC5396815          DOI: 10.5152/TurkPediatriArs.2017.2513

Source DB:  PubMed          Journal:  Turk Pediatri Ars


  49 in total

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Authors:  M Zakarija; J M McKenzie
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Journal:  Eur J Pediatr       Date:  1985-03       Impact factor: 3.183

9.  Iodine overload and severe hypothyroidism in two neonates.

Authors:  Selim Kurtoğlu; Leyla Akın; Mustafa Ali Akın; Dilek Çoban
Journal:  J Clin Res Pediatr Endocrinol       Date:  2009-11-05

10.  European Society for Paediatric Endocrinology consensus guidelines on screening, diagnosis, and management of congenital hypothyroidism.

Authors:  Juliane Léger; Antonella Olivieri; Malcolm Donaldson; Toni Torresani; Heiko Krude; Guy van Vliet; Michel Polak; Gary Butler
Journal:  J Clin Endocrinol Metab       Date:  2014-01-21       Impact factor: 5.958

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Journal:  Turk Pediatri Ars       Date:  2017-12-01

3.  MATERNAL GRAVES DISEASE AND ABNORMAL CYP2D6 GENOTYPE WITH FETAL HYPERTHYROIDISM.

Authors:  Christopher Spoke; Christopher Martin
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4.  TSHRV656F Activating Variant of the Thyroid Stimulating Hormone Receptor Gene in Neonatal Onset Hyperthyroidism: A Case Review

Authors:  Leman Kayaş; Emine Çamtosun; Ayşehan Akıncı; Rıfat Bircan
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