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CASE REPORT
Ochronotic spondylosis of 5 years old boy – a case report
Ochronotic spondylosis of 5 years old boy – a case report
Online publication date: 2006-02-15
Reumatologia 2006;44(1):52-55
KEYWORDS
ABSTRACT
Alkaptonuria is a rare disorder caused by congenital homogentisate oxidaze deficiency of recessive inheritance. Homogentisate polymers are accumulated and manifested with urine darkening and ochronosis.
A 12 years case history of a boy aged 17 with intervertebral disc calcification intractu ochronosis is presented. The clinical picture, diagnostic and therapeutic possibilities are described.
Copyright: © Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie. This is an Open Access journal, all articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (https://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
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| eISSN: | 2084-9834 |
| ISSN: | 0034-6233 |
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