Ochronotic spondylosis of 5 years old boy - a case report
Journal Title: Reumatologia - Year 2006, Vol 44, Issue 1
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.
Authors and Affiliations
Lidia Rutkowska-Sak, Iwona Słowińska, Beata Kołodziejczyk
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