Glomerulopathy with fibronectin deposits

11/01/2021 - "Prednisone-induced sustained remission in a patient with familial fibronectin glomerulopathy (GFND)."

10/16/2023 - "These findings established the diagnosis of recurrent fibronectin glomerulopathy secondary to a novel variant in the fibronectin 1 gene. "
10/01/2023 - "Fibronectin glomerulopathy (FNG) is an autosomal dominant disease, and nearly half of patients are involved in a mutation of the fibronectin gene (FN1). "
11/30/2022 - "Fibronectin glomerulopathy is a rare, familial glomerular disease characterized by mesangial fibronectin deposition in the glomeruli. "
03/30/2018 - "Fibronectin glomerulopathy is a rare autosomal dominant inherited glomerular disease associated with massive deposition of fibronectin. "
03/30/2018 - "Fibronectin Glomerulopathy Caused by the Y973C Mutation in Fibronectin: A Case Report and Literature Review."

11/30/2022 - "Herein, we report a case of fibronectin glomerulopathy presenting as strong IgA and C3 immunostaining in renal biopsy, concomitant with monoclonal gammopathy (monoclonal IgA κ). "
01/01/2013 - "Clinicopathological analysis of glomerulopathy with fibronectin deposits (GFND): a case of sporadic, elderly-onset GFND with codeposition of IgA, C1q, and fibrinogen."

11/01/2017 - "Familial microscopic hematuria (FMH) is associated with a genetically heterogeneous group of conditions including the collagen-IV nephropathies, the heritable C3/CFHR5 nephropathy and the glomerulopathy with fibronectin deposits. "
02/01/1998 - "amyloidosis, immunotactoid glomerulopathy, light-chain glomerulopathy, cryoglobulinaemia, collagen-III glomerulopathy, fibronectin glomerulopathy) could be excluded. "

03/01/2022 - "Bortezomib-containing regiment in treating glomerulopathy with fibronectin deposits combined with monoclonal gammopathy of undetermined significance: a case report and literature review."
11/30/2022 - "Fibronectin glomerulopathy with monoclonal gammopathy responding to bortezomib plus dexamethasone: a case report."

06/01/2010 - "The following disorders are discussed by mode of inheritance: 1) Autosomal dominant: autosomal dominant polycystic kidney disease, nephropathies associated with uromodulin (medullary cystic disease and familial juvenile hyperuricemic nephropathy), renal cysts and diabetes syndrome, nail-patella syndrome, glomerulopathy with fibronectin deposits. "

11/01/1996 - "These three distinct forms of glomerulopathy include collagen type III glomerulopathy, fibronectin glomerulopathy, and lipoprotein glomerulopathy. "

11/01/1996 - "Collagen type II and fibronectin glomerulopathy are familial diseases, and lipoprotein glomerulopathy may be familial or sporadic."

05/01/2012 - "The proteomes of glomeruli isolated by laser capture microdissection from biopsies of normal kidneys (living-related donor kidneys) were compared with those from patients with diabetic nephropathy, lupus nephritis, and fibronectin glomerulopathy. "

09/01/1998 - "Exclusion of the uteroglobin gene as a candidate for fibronectin glomerulopathy (GFND)"

05/01/2012 - "The proteomes of glomeruli isolated by laser capture microdissection from biopsies of normal kidneys (living-related donor kidneys) were compared with those from patients with diabetic nephropathy, lupus nephritis, and fibronectin glomerulopathy. "