z-logo
open-access-imgOpen Access
A Case of Immunotactoid Glomerulopathy with Rapid Progression to End-Stage Renal Disease
Author(s) -
Shikha Jain,
Darshika Chhabra
Publication year - 2009
Publication title -
the scientific world journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.453
H-Index - 93
eISSN - 2356-6140
pISSN - 1537-744X
DOI - 10.1100/tsw.2009.164
Subject(s) - glomerulopathy , medicine , end stage renal disease , renal biopsy , disease , pathology , cryoglobulinemia , amyloidosis , stage (stratigraphy) , kidney disease , biopsy , glomerulonephritis , kidney , immunology , biology , paleontology , hepatitis c virus , virus
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.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom