Concurrent mucous membrane pemphigoid and membranous glomerulonephritis in a patient with autoantibodies targeting the 1080 region of collagen XVII
Author:
Affiliation:
1. Department of Dermatology Roy J. and Lucille A. Carver College of Medicine, University of Iowa, and Veterans Administration Medical Center Iowa City Iowa U.S.A.
Publisher
Wiley
Subject
Dermatology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjd.17923
Reference8 articles.
1. A case of subepidermal blistering disease with autoantibodies to multiple laminin subunits who developed later autoantibodies to alpha‐5 chain of type IV collagen associated with membranous glomerulonephropathy;Sueki H;Acta Derm Venereol,2015
2. Bullous Pemphigoid With a Dual Pattern of Glomerular Immune Complex Disease
3. Missing the target: Characterization of bullous pemphigoid patients who are negative using the BP180 enzyme-linked immunosorbant assay
4. Phospholipase A2 receptor staining is absent in many kidney biopsies with early-stage membranous glomerulonephritis
5. Transmembrane collagen XVII is a novel component of the glomerular filtration barrier
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1. Pemphigus vulgaris and focal segmental glomerulosclerosis (FSGS): First reported case and a review of the literature;Clinical Case Reports;2023-07
2. Use of rituximab in the treatment of mucous membrane pemphigoid: An analytic review;Autoimmunity Reviews;2022-08
3. A Case of Severe and Refractory Membranous Nephropathy Associated to Mucous Membrane Pemphigoid;Case Reports in Nephrology;2021-05-11
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