Volume 19, Number 4 (winter 2009)                   J Urmia Univ Med Sci 2009, 19(4): 353-355 | Back to browse issues page


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A CASE REPORT OF ALKAPTONURIC OCHRONOSIS. J Urmia Univ Med Sci. 2009; 19 (4) :353-355
URL: http://umj.umsu.ac.ir/article-1-363-en.html

Abstract:   (8363 Views)

  F Abbasi [1] , Ph.D S Naji [2] , Ph.D F Mirzatolui [3] , MD G Behjati [4] , Ph.D

 

 Received: 28 April, 2008 Accepted: 5 Nov, 2008

 Abstract

  Alkaptonuria is a rare autosomal recessive disorder characterized by deficiency of homogentisic acid oxidase. This deficiency leads to accumulation of homogentisic acid in tissues and its urinary excretion and resulting in characteristic features like ochronosis, darkening of urine, and arthropathy. We describe a case of alkaptonuric ochronosis in a 62 year old man, who had alkaptonuria, degenerative arthropathy of hip and knees, spinal abnormalities similar to ankylosing spondylitis and renal calculi.Total replacement of hip joint was done. Total replacement of hip joint was done.

 

  Keywords: Alkaptonuria, Ochronosis, Degenerative arthropathy

 

  Address: Imam Khomeni Hospital , Urmia Tel: 09141452352

 

  E-mail: faribaak2002@yahoo.com

 

  Source: UMJ 2009: 19(4): 367 ISSN: 1027-3727



  [1] Assistant Professor of Pathology, Urmia University of Medical Sciences (Corresponding Author)

  [2] Assistant Professor of Pathology, Urmia University of Medical Sciences

  [3] Associate Professor of Orthopedics, Urmia University of Medical Sciences

  [4] Specialist in Pathology, Legal Medicine Center of Isfahan

Full-Text [PDF 201 kb]   (940 Downloads)    
Subject: آناتومی
Received: 2009/03/14

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