Suppr超能文献

厄瓜多尔罕见变异遗传性淀粉样变性的病例报告

Experience of Hereditary Amyloidosis with Rare Variant in Ecuador: Case Reports.

机构信息

Hospital General Manuel Ygnacio Monteros-IESS, Loja 110150, Ecuador.

Heredity S.A., Quito 170135, Ecuador.

出版信息

Med Sci (Basel). 2024 Oct 21;12(4):58. doi: 10.3390/medsci12040058.

Abstract

More than approximately 120 transthyretin mutations are known. Their clinical presentation is heterogeneous, as the course of disease onset depends on genetic variation and level of penetrance. They are little known in Ecuador, and some of the reported cases suggest-given analysis of family trees-that they come from a province that is possibly considered endemic. The main objective of this study is to perform a descriptive observational analysis on the presentation of transthyretin amyloidosis in families carrying the p.Ser43Asn gene of the identified index case.

摘要

已知超过约 120 种转甲状腺素蛋白突变。其临床表现具有异质性,因为疾病发作的病程取决于遗传变异和外显率。在厄瓜多尔,这些突变并不广为人知,一些报告的病例表明——通过对家族树的分析——它们可能来自一个被认为是地方性的省份。本研究的主要目的是对携带已确定索引病例的 p.Ser43Asn 基因的家族中转甲状腺素蛋白淀粉样变性的表现进行描述性观察分析。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验