A CF patient with progressive proteinuric renal disease: A CF-specific nodular glomerulosclerosis?

6Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Cystic fibrosis (CF) is a multisystemic disease but without a classical disease-specific renal phenotype. A 32-year-old male patient with CF (ΔF508/ΔF508) presented with a nephrotic syndrome. Renal biopsy revealed nodular glomerulosclerosis (NGS) occurring in the absence of diabetes mellitus, amyloidosis and any other known common cause of NGS. He had a progressive decline in estimated glomerular filtration rate (eGFR) to chronic kidney disease stage V (eGFR <15 mL/min/1.73 m2) over a 3-year period despite optimal medical management. This is the fourth reported case of NGS in a patient with CF without diabetes and is the first to originate from a European country. This case supports the concept of a CF-related NGS. © 2010 The Author.

Cite

CITATION STYLE

APA

O’Connell, O., Magee, C. N., Fitzgerald, B., Burke, L., Plant, W. D., & Plant, B. J. (2010). A CF patient with progressive proteinuric renal disease: A CF-specific nodular glomerulosclerosis? NDT Plus, 3(4), 354–356. https://doi.org/10.1093/ndtplus/sfq054

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