首页> 美国卫生研究院文献>The Journal of Clinical Endocrinology and Metabolism >A Single Copy of the Recently Identified Dual Oxidase Maturation Factor (DUOXA) 1 Gene Produces Only Mild Transient Hypothyroidism in a Patient with a Novel Biallelic DUOXA2 Mutation and Monoallelic DUOXA1 Deletion
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A Single Copy of the Recently Identified Dual Oxidase Maturation Factor (DUOXA) 1 Gene Produces Only Mild Transient Hypothyroidism in a Patient with a Novel Biallelic DUOXA2 Mutation and Monoallelic DUOXA1 Deletion

机译:最近鉴定出的双氧化酶成熟因子(DUOXA)1基因的单拷贝在新型双等位基因DUOXA2突变和单等位基因DUOXA1缺失的患者中仅产生轻度短暂甲状腺功能减退

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摘要

Context:Dual oxidases (DUOX1 and DUOX2) play a crucial role in the generation of hydrogen peroxide required in the oxidation of iodide and the synthesis of thyroid hormone. Heterodimerization with specific maturation factors (DUOXA1 and DUOXA2) is essential for the maturation and function of the DUOX enzyme complexes. Biallelic loss-of-function mutations of DUOX2 result in congenital hypothyroidism (CH), whereas a single reported case of homozygous DUOXA2 mutation (Y246X) has been associated with mild CH.
机译:背景:双重氧化酶(DUOX1和DUOX2)在碘化物的氧化和甲状腺激素的合成中所需的过氧化氢的产生中起着至关重要的作用。具有特定成熟因子(DUOXA1和DUOXA2)的异源二聚化对于DUOX酶复合物的成熟和功能至关重要。 DUOX2的双等位基因功能丧失突变导致先天性甲状腺功能减退症(CH),而纯合性DUOXA2突变(Y246X)的单个报道病例与轻度CH相关。

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