A case of immunotactoid glomerulopathy with rapid progression to end-stage renal disease

5Citations
Citations of this article
19Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Immunotactoid glomerulopathy (IGN) is a rare immunoglobulin deposition disease. It is often mistaken for cryoglobulinemia or amyloidosis due to the similarities on biopsy findings. The disease progresses to end-stage renal disease (ESRD) within 7 months to 10 years. This is the first case reported of a patient with a diagnosis of IGN who developed acute kidney injury (AKI) and ESRD within 1 week of initial presentation. ©2009 with author.

Cite

CITATION STYLE

APA

Jain, S., & Chhabra, D. (2009). A case of immunotactoid glomerulopathy with rapid progression to end-stage renal disease. TheScientificWorldJournal, 9, 1348–1354. https://doi.org/10.1100/tsw.2009.164

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free