Ochronotic Chronic Tendoachilles Rupture Management: A Case Series

Background: Alkaptonuria is a rare inherited genetic disorder in which there is a deficiency of the enzyme homogentisate 1,2-dioxygenase. The three characteristics of alkaptonuria are homogentisic-aciduria, ochronosis, and ochronotic arthropathy. Alkaptonuria is usually asymptomatic until the third...

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Bibliographic Details
Main Authors: Jeremy B Dorai, Issac Jebaraj
Format: Article
Language:English
Published: Jaypee Brothers Medical Publisher 2024-12-01
Series:Journal of Foot and Ankle Surgery (Asia Pacific)
Subjects:
Online Access:https://www.jfasap.com/doi/JFASAP/pdf/10.5005/jp-journals-10040-1363
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