A recurrent fibronectin glomerulopathy in a renal transplant patient: a case report
Author:
Affiliation:
1. Department of Nephrology and Transplantation Center; Japanese Red Cross Nagoya Daini Hospital; Nagoya; Japan
2. Institute for Pathology; University of Basel; Basel; Switzerland
3. Division of Pathology; Sendai Shakaihoken Hospital; Sendai; Japan
Publisher
Wiley
Subject
Transplantation
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0012.2012.01644.x/fullpdf
Reference13 articles.
1. A unique familial lobular glomerulopathy;Tuttle;Arch Pathol Lab Med,1987
2. Glomerulonephritis with organized deposits: a mesangiopathic, not immune complex-mediated disease?. A pathologic study of two cases in the same family;Mazzucco;Hum Pathol,1992
3. Familial glomerulonephritis characterized by massive deposits of fibronectin;Assmann;Am J Kidney Dis,1995
4. Glomerulopathy associated with predominant fibronectin deposits: a newly recognized hereditary disease;Strøm;Kidney Int,1995
5. Familial glomerulopathy with giant fibrillar (fibronectin-positive) deposits: 15-year follow-up in a large kindred;Gemperle;Am J Kidney Dis,1996
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2. Pathologic-genomic correlation identified a novel variant in FN1 and established the diagnosis of recurrent fibronectin glomerulopathy in the kidney allograft;American Journal of Transplantation;2023-10
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4. A child with genetic FN1 mutation in the absence of classic glomerulopathy with fibronectin deposits(GFND) findings on biopsy;BMC Nephrology;2022-07-14
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