Literature DB >> 25331409

[Hereditary fibrinogen Aα-chain amyloidosis caused by the E526V mutation: a case report and literature review].

Ying Yao1, Su-xia Wang1, You-kang Zhang1.   

Abstract

Mutations in the fibrinogen Aα-chain genes are the most common cause of hereditary renal amyloidosis. The renal histologic appearance in the patient is characteristic and shows striking glomerular enlargement with almost complete obliteration of the normal glomerular architecture by extensive amyloid deposition. In contrast, the vessels and renal tubular interstitium of such patient contains almost no amyloid at all. Here, we described a patient with hereditary fibrinogen amyloidosis, who presented with proteinuria, hypertension and renal failure. He was shown to be heterozygous for the relevant mutation encoding the E526V fibrinogen variant.

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Year:  2014        PMID: 25331409

Source DB:  PubMed          Journal:  Beijing Da Xue Xue Bao Yi Xue Ban        ISSN: 1671-167X


  3 in total

Review 1.  Hereditary Fibrinogen Aα-Chain Amyloidosis in Asia: Clinical and Molecular Characteristics.

Authors:  Masahide Yazaki; Tsuneaki Yoshinaga; Yoshiki Sekijima; Fuyuki Kametani; Nobuo Okumura
Journal:  Int J Mol Sci       Date:  2018-01-22       Impact factor: 5.923

2.  Typing of hereditary renal amyloidosis presenting with isolated glomerular amyloid deposition.

Authors:  Danyang Li; Dan Liu; Hui Xu; Xiao-Juan Yu; Fu-de Zhou; Ming-Hui Zhao; Su-Xia Wang
Journal:  BMC Nephrol       Date:  2019-12-23       Impact factor: 2.388

3.  Fibrinogen A Alpha-Chain Amyloidosis in Two Chinese Patients.

Authors:  Zhen-Yu Li; Shuang Wang; Dan-Yang Li; Dan Liu; Su-Xia Wang; Xiao-Juan Yu; Gang Liu; Fu-De Zhou; Ming-Hui Zhao
Journal:  Front Med (Lausanne)       Date:  2022-04-28
  3 in total

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