由杂合c148G >a p.Val50Leu突变引起的变异型转甲状腺蛋白淀粉样心肌病患者二头肌近端长肌腱部分断裂

Belma Kalaycı, Ezgi Polat Ocaklı, Nur Aydınbelge Dizdar, Esin Kurtuluş Öztürk, Taha Bahsi, Özlem Özmen
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引用次数: 0

摘要

变异型转甲状腺素淀粉样心肌病(attv - cm)是一种由ATTR基因突变引起的罕见疾病。由于致病性突变,转甲状腺素四聚体失去其结构稳定性和错误折叠,导致淀粉样蛋白原纤维在各种组织中积累,特别是在心脏中。ATTRv-CM的临床进展取决于特定的突变。关于基耶病毒中ATTR基因突变的数据有限。本文报道一例自发性肱二头肌肌腱断裂,在诊断前确诊,患者为携带杂合c148G> a pVal50Leu突变的ATTRv-CM患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spontaneous Partial Rupture of the Long Proximal Biceps Tendon in a Patient with Variant Transthyretin Amyloid Cardiomyopathy Due to a Heterozygous c148G>A p.Val50Leu Mutation.

Variant transthyretin amyloid cardiomyopathy (ATTRv-CM) is a rare disease caused by a genetic mutation in the ATTR gene. Due to the pathogenic mutation, transthyretin tetramers lose their structural stability and misfold, leading to the accumulation of amyloid fibrils in various tissues, particularly in the heart. The clinical progression of ATTRv-CM varies depending on the specific mutation. Data on ATTR gene mutations in Türkiye are limited. This paper presents a case of spontaneous biceps tendon rupture, identified prior to diagnosis, in a patient with ATTRv-CM carrying a heterozygous c148G>A pVal50Leu mutation.

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