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淀粉样变性,一种神秘的疾病,仍然被低估。

Amiloidosis, a mysterious disease, still underestimated.

作者信息

Penescu Mircea

机构信息

Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.

出版信息

J Med Life. 2008 Apr-Jun;1(2):189-97.

Abstract

Amyloidosis, 150 years after being identified, still remains a mysterious disease, full of mystery, question marks and challenges, almost always ignored from the start, with terrible symptoms and terrible prognosis. The mechanics of the formation. persistence and setting of the amyloid fibrils are still under discussion. This article wishes to point out some of the main characteristics of this disease and the involved proteins by referring to the history. The pathogenesis, the histology, the diagnosis and a few aspects of the prognosis of this disease in the hope that future research will bring to light the answers for the mystery of amyloidosis along with more efficient therapies.

摘要

淀粉样变性在被发现150年后,仍然是一种神秘的疾病,充满了谜团、问号和挑战,几乎从一开始就被忽视,伴有可怕的症状和糟糕的预后。淀粉样纤维的形成、持续存在和沉积机制仍在讨论中。本文希望通过回顾历史指出这种疾病的一些主要特征以及相关蛋白质。阐述这种疾病的发病机制、组织学、诊断及预后的几个方面,以期未来的研究能够揭开淀粉样变性之谜并带来更有效的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/100a/5654071/9b228936494d/JMedLife-1-189-g001.jpg

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