Volume 29, Issue 1 (3-2005)                   Research in Medicine 2005, 29(1): 67-69 | Back to browse issues page

XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Ghojevand N. Research in Medicine. 2005; 29 (1) :67-69
URL: http://pejouhesh.sbmu.ac.ir/article-1-60-en.html
Abstract:   (10642 Views)
Conorenal syndrome or Saldino Mainzer is a rare hereditary disease characterized by cone-shaped epiphyses of the phalanges, retinitis pigmentosa and renal manifestations (nephropathy). Case report: Herein we report an eight years old girl with a collection of signs and symptoms compatible with conorenal syndrome. She first presented with dactylitis, dysuria, frequency, discolored urine and progressive generalized edema. Renal biopsy revealed tubular atrophy, interstitial fibrosis and thickening of the glomerular basement membrane. This constellation of signs and symptoms is compatible with conorenal syndrome.
Full-Text [PDF 123 kb]   (1731 Downloads)    
Type of Study: General | Subject: General
Received: 2003/11/27

Creative Commons License
This Journal is licensed under a Creative Commons Attribution 4.0 International License  | Research in Medicine

Designed & Developed by : Yektaweb