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
Ghojevand N
Abstract:   (15076 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.
Keywords: KEYWORDS: Conorenal syndrome, Saldino Mainzer, Multiple epiphyseal dysplasia, Retinitis Pigmentosa, children.
Full-Text [PDF 123 kb]   (3047 Downloads)    
Type of Study: General | Subject: Interdisciplinary (Educational Management, Educational research, Statistics, Medical education
Received: 2003/11/27 | Published: 2005/03/15
Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

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

Designed & Developed by : Yektaweb