A CASE REPORT OF ALKAPTONURIC OCHRONOSIS

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ABBASI F.; NAJI S.; MIRZATOLOUEI FARDIN; BEHJATI GH.R.

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Journal: Studies in Medical Sciences Year:2009 | Volume:19 | Issue:4 Page(s): 353-355

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Title

A CASE REPORT OF ALKAPTONURIC OCHRONOSIS

Author(s)

ABBASI F. | NAJI S. | MIRZATOLOUEI FARDIN | BEHJATI GH.R. | Issue Writer Certificate

Keywords

ALKAPTONURIAQ3

OCHRONOSISQ3

DEGENERATIVE ARTHROPATHYQ3

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.

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APA: Copy

ABBASI, F., NAJI, S., MIRZATOLOUEI, FARDIN, & BEHJATI, GH.R.. (2009). A CASE REPORT OF ALKAPTONURIC OCHRONOSIS. STUDIES IN MEDICAL SCIENCE (THE JOURNAL OF URMIA UNIVERSITY OF MEDICAL SCINCES), 19(4), 353-355. SID. https://sid.ir/paper/63851/en

Vancouver: Copy

ABBASI F., NAJI S., MIRZATOLOUEI FARDIN, BEHJATI GH.R.. A CASE REPORT OF ALKAPTONURIC OCHRONOSIS. STUDIES IN MEDICAL SCIENCE (THE JOURNAL OF URMIA UNIVERSITY OF MEDICAL SCINCES)[Internet]. 2009;19(4):353-355. Available from: https://sid.ir/paper/63851/en

IEEE: Copy

F. ABBASI, S. NAJI, FARDIN MIRZATOLOUEI, and GH.R. BEHJATI, “A CASE REPORT OF ALKAPTONURIC OCHRONOSIS,” STUDIES IN MEDICAL SCIENCE (THE JOURNAL OF URMIA UNIVERSITY OF MEDICAL SCINCES), vol. 19, no. 4, pp. 353–355, 2009, [Online]. Available: https://sid.ir/paper/63851/en

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