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An Ex vivo Culture System to Study Thyroid Development
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与甲状腺在位的先天性甲状腺功能低下症:NKX2-1和DUOX2低形变体的病例报告
Erika Uehara1,2, Naoaki Hori3, Kanako Tanase-Nakao4
1Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan, uehara-e@ncchd.go.jp.
Hormone research in paediatrics
|April 18, 2024
概括
在NKX2-1和DUOX2中的遗传变异可以导致过渡性先天性甲状腺功能低下症 (CH). 一种部分功能丧失的NKX2-1变体与DUOX2变体相结合,导致患者的CH与高甲状腺蛋白水平.
科学领域:
- 内分泌学 在内分泌学.
- 遗传学 遗传学 是一个
背景情况:
- 出生性甲状腺功能低下症 (CH) 随着激素生成越来越多地被报告,通常涉及多种遗传变异.
- 在甲状腺激素合成中,NK2本体盒1 (NKX2-1) 和双氧化酶2 (DUOX2) 是关键基因.
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