DUOX2 variants are a frequent cause of congenital primary hypothyroidism in Thai patients

DUOX2 variants are a frequent cause of congenital primary hypothyroidism in Thai patients

Objective: To identify the genetic etiologies of congenital primary hypothyroidism (CH) in Thai patients. Design and methods: CH patients were enrolled. Clinical characteristics including age, signs and symptoms of CH, pedigree, family history, screened thyroid-stimulating hormone results, thyroi...

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Main Authors: Kinnaree Sorapipatcharoen, Thipwimol Tim-Aroon, Pat Mahachoklertwattana, Wasun Chantratita, Nareenart Iemwimangsa, Insee Sensorn, Bhakbhoom Panthan, Poramate Jiaranai, Saisuda Noojarern, Patcharin Khlairit, Sarunyu Pongratanakul, Chittiwat Suprasongsin, Manassawee Korwutthikulrangsri, Chutintorn Sriphrapradang, Preamrudee Poomthavorn
Format: Article
Language:English
Published: Bioscientifica 2020-12-01
Series:Endocrine Connections
Subjects:
congenital hypothyroidism
next generation sequencing
duox2
thyroid dyshormonogenesis
thyroid dysgenesis
goiter
Online Access:https://ec.bioscientifica.com/view/journals/ec/aop/ec-20-0411/ec-20-0411.xml

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https://ec.bioscientifica.com/view/journals/ec/aop/ec-20-0411/ec-20-0411.xml

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