CASE REPORT<BR>Ochronotic spondylosis of 5 years old boy – a case report

Lidia Rutkowska-Sak; Iwona Słowińska; Beata Kołodziejczyk

eISSN: 2084-9834
ISSN: 0034-6233

Reumatologia/Rheumatology

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1/2006
vol. 44

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abstract:

CASE REPORT
Ochronotic spondylosis of 5 years old boy – a case report

Lidia Rutkowska-Sak

,

Iwona Słowińska

,

Beata Kołodziejczyk

rU 2006; 44, 1: 52-55

Online publish date: 2006/02/15

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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.

keywords:

alkaptonuria, ochronotic changes, children

EVENTS/KONFERENCJE

BOOKS/KSIĄŻKI

CASE REPORTOchronotic spondylosis of 5 years old boy – a case report

Lidia Rutkowska-Sak , Iwona Słowińska , Beata Kołodziejczyk

alkaptonuria, ochronotic changes, children

CASE REPORT
Ochronotic spondylosis of 5 years old boy – a case report

Lidia Rutkowska-Sak

,

Iwona Słowińska

,

Beata Kołodziejczyk