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Updated: Feb 20, 2026

Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
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系统性表现和 Transthyretin V142I 变种载体的死亡风险:一百万退伍军人计划分析分析

Konstantinos Sideris1, Tyler J Nelson2, Lina Brinker1

  • 1Department of Internal Medicine, George E. Wahlen Department of Veterans Affairs Medical Center, Salt Lake City, Utah, USA; Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.

JACC. CardioOncology
|February 18, 2026
PubMed
概括

该TTR V142I变体显著增加了心力衰竭,心肌病和其他疾病的风险,如心房动和神经病变在非洲血统的个人. 早期诊断对于管理这种对粉样性病的遗传倾向至关重要.

关键词:
V142II 这是一本小说.氨基粉症是什么?心房动是心房动的一种.心肌病性心脏病 - 心肌病性心脏病带道综合征是什么意思遗传学 遗传学 遗传学 是一个神经病变是一种神经病变.脊柱狭窄症 脊柱狭窄症 脊柱狭窄症变异型的 transthyretin 氨基化症.

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