A clinical case of late diagnosis of ochronosis

DOI: https://doi.org/10.29296/25877305-2019-11-15
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Issue: 
11
Year: 
2019

V. Chupakhina(1), Candidate of Medical Sciences; T. Bolshakova(1), Candidate of Medical Sciences; E. Kapustina(1, 2), Candidate of Medical Sciences; T. Potupchik(1), Candidate of Medical Sciences; L. Boeva(1, 2), Candidate of Medical Sciences; T. Pasechnik(2); I. Shilova(2); G. Bulygin(3); A. Budarev(3) 1-Prof. V.F. Voino-Yasenetsky Krasnoyarsk State Medical University; 2-Territorial Clinical Hospital, Krasnoyarsk 3-A.I. Kryzhanovsky Krasnoyarsk Territorial Clinical Oncology Dispensary

The paper describes a clinical case of a 56-year-old woman with ochronosis, a rare inherited metabolic disease. It considers the clinical manifestations of ochronosis, methods for its diagnosis, and the features of treatment.
Keywords: 
rheumatic diseases
ochronosis
homogentisic acid
alkaptonuria
chondrocalcinosis
nitisinone

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