Results 1 to 10 of about 62,552 (281)

C3 glomerulopathies: dense deposit disease and C3 glomerulonephritis [PDF]

open access: yesFrontiers in Medicine, 2023
Dense deposit disease (DDD) and C3 glomerulonephritis (C3GN) are types of membranoproliferative glomerulonephritis classified as C3 glomerulopathies.
Claudio Ponticelli   +4 more
doaj   +4 more sources

A long history of dense deposit disease [PDF]

open access: yesBMC Ophthalmology, 2018
Background Dense Deposit Disease is a rare condition affecting the Bruch’s membrane and the glomerular basement membrane. We report the progression of the ocular manifestations over a 30 year follow up period, longer than any previous report.
Alan Cunningham, Ajay Kotagiri
doaj   +5 more sources

Blockade of Alternative Complement Pathway in Dense Deposit Disease [PDF]

open access: yesCase Reports in Nephrology, 2014
A patient aged 17 with dense deposit disease associated with complement activation, circulating C3 Nef, and Factor H mutation presented with nephrotic syndrome and hypertension.
Aurore Berthe-Aucejo   +6 more
doaj   +5 more sources

A Child with Dense Deposit Disease and Decreased Classic Complement Pathway Activity [PDF]

open access: yesActa Clinica Croatica, 2021
We report a rare case of nephritic syndrome underlying dense deposit disease (DDD) with alternative complement pathway dysfunction explained with both C3 nephritic factor (C3NeF) antibodies and DDD associated polymorphism of factor H. An 8-year-old boy
Ivana Trutin   +4 more
doaj   +2 more sources

The Retinal Complications of C3 Dense Deposit Disease: A Scoping Review [PDF]

open access: yesVision
People with C3 Dense Deposit Disease (C3DDD), a rare autoimmune disease, often also have ocular complications. Due to the rarity of this disease, there is little known about ocular complications in populations across the world. This paper aimed to assess
Jolene McCarney   +4 more
doaj   +2 more sources

Iptacopan treatment for recurrent dense deposit disease after kidney transplant: A case report [PDF]

open access: yesSAGE Open Medical Case Reports
C3 glomerulopathies, including dense deposit disease, are rare kidney disorders caused by dysregulation of the alternative complement pathway. Recurrence after kidney transplantation is common and can threaten graft survival.
Lean AlKhatib   +3 more
doaj   +2 more sources

Case report: a rare concurrence of dense deposit disease in an adolescent patient with IgA nephropathy [PDF]

open access: yesBMC Pediatrics
Background Dense deposit disease (DDD) is a rare renal disorder major affecting adolescents and children, characterized by an absence of distinctive clinical symptoms.
Jian-Hui Zhang   +6 more
doaj   +2 more sources

Favorable effect of bortezomib in dense deposit disease associated with monoclonal gammopathy: a case report [PDF]

open access: yesBMC Nephrology, 2018
Background Complement component 3 (C3) glomerulopathy, which includes dense deposit disease (DDD) and C3 glomerulonephritis, is caused by dysregulation of the alternative complement pathway.
Shuma Hirashio   +7 more
doaj   +2 more sources

A case of regression of atypical dense deposit disease without C3 deposition in a child [PDF]

open access: yesKorean Journal of Pediatrics, 2010
Dense deposit disease (DDD) is a rare disorder characterized by the deposition of abnormal electron-dense material within the glomerular basement membrane of the kidneys. The diagnosis is made in most patients between 5 and 15 years of age, and within 10
Min Sun Kim   +3 more
doaj   +2 more sources

Primary membranoproliferative glomerulonephritis: natural history, pathogenesis, and treatment [PDF]

open access: yesFrontiers in Nephrology
Primary membranoproliferative glomerulonephritis (MPGN) is an ultrarare disease characterized by immunofluorescence microscopy as either immune-complex mediated (IC-MPGN) or C3 glomerulopathy (C3), the latter subdivided by electron microscopy to C3 ...
Edward J. Filippone, John L. Farber
doaj   +2 more sources

Home - About - Disclaimer - Privacy