| Literature DB >> 25423645 |
Mehreen Adhi, Sarah P Read, Jonathan J Liu, James G Fujimoto, Jay S Duker.
Abstract
Membranoproliferative glomerulonephritis (MPGN) type 2 is characterized by electron-dense deposits in the glomerular basement membrane and drusen-like deposits in Bruch's membrane. Over time, atrophic changes in the retina and retinal pigment epithelium occur, which can progress to choroidal neovascularization (CNV). This report describes a patient with MPGN type 2 who developed progressive loss of vision secondary to CNV. High-speed ultrahigh-resolution optical coherence tomography (UHR-OCT) showed an irregular Bruch's membrane that measured 10 μm beneath the foveal center. High-speed UHR-OCT can potentially be used to analyze Bruch's membrane in secondary ocular manifestations of diseases such as MPGN type 2 and primary retinal diseases such as age-related macular degeneration. Copyright 2014, SLACK Incorporated.Entities:
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Year: 2014 PMID: 25423645 PMCID: PMC4712916 DOI: 10.3928/23258160-20141118-20
Source DB: PubMed Journal: Ophthalmic Surg Lasers Imaging Retina ISSN: 2325-8160 Impact factor: 1.300