Rare case alert: Ochronotic arthropathy and its skeletal manifestations in 2 Indian siblings

Rare case alert: Ochronotic arthropathy and its skeletal manifestations in 2 Indian siblings

Alkaptonuria is a rare inborn error of metabolism disorder, with an incidence of one in a million births presenting with a triad of dark staining of urine, ochronosis, and Spondyloarthropathy. Till date, 1233 cases have been reported. Ochronotic arthropathy has often been a “serendipity,” with most...

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Bibliographic Details
Main Authors: Sherashah F Kammar, Adiveppa A Hosangadi, Hemanth D Ramaiah
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2023-01-01
Series:Journal of Orthopaedics and Spine
Subjects:
alkaptonuria
homogentisate oxidase deficiency
ochronosis
ochronotic arthropathy
spondyloarthropathy
Online Access:http://www.joas.org.in/article.asp?issn=2666-7150;year=2023;volume=11;issue=1;spage=35;epage=39;aulast=Kammar

Internet

http://www.joas.org.in/article.asp?issn=2666-7150;year=2023;volume=11;issue=1;spage=35;epage=39;aulast=Kammar

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