Clinicopathological Analysis of Glomerulopathy with Fibronectin Deposits (GFND): A Case of Sporadic, Elderly-Onset GFND with Codeposition of IgA, C1q, and Fibrinogen
Author:
Affiliation:
1. Division of Nephrology and Rheumatology, Department of Internal Medicine, Aichi Medical University School of Medicine, Japan
2. Division of Nephrology, Ise Red Cross Hospital, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/52/15/52_52.0046/_pdf
Reference20 articles.
1. 1. Mazzucco G, Maran E, Rollino C, Monga G. Glomerulonephritis with organized deposits: a mesangiopathic, not immune complex-mediated disease? A pathologic study of two cases in the same family. Hum Pathol 23: 63-68, 1992.
2. 2. Strøm EH, Banfi G, Krapf R, et al. Glomerulopathy associated with predominant fibronectin deposits: a newly recognized hereditary disease. Kidney Int 48: 163-170, 1995.
3. 3. Castelletti F, Donadelli R, Banterla F, et al. Mutations in FN1 cause glomerulopathy with fibronectin deposits. Proc Natl Acad Sci U S A 105: 2538-2543, 2008.
4. 4. Pankov R, Yamada KM. Fibronectin at a glance. J Cell Sci 115 (Pt 20): 3861-3863, 2002.
5. 5. Mao Y, Schwarzbauer JE. Fibronectin fibrillogenesis, a cell-mediated matrix assembly process. Matrix Biol 24: 389-399, 2005.
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