Alkaptonuria: Spontaneous Achilles tendon rupture: Case report.

E. Baca, A. Kural, N. Ziroğlu, Cemal Kural
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引用次数: 4

Abstract

Alkaptonuria is an autosomal recessive disease caused by the accumulation of homogentisic acid (HGA) products in the ligament, cartilage, skin and various organs due to the lack of HGA oxidase enzyme. In this article, we present a 61-year-old male patient operated on due to a diagnosis of spontaneous Achilles tendon rupture and diagnosed as alkaptonuria due to the intraoperative color of the tissues and the subsequent examinations. We also reviewed alkaptonuria and its accompanying pathologies in light of the literature.
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尿尿:自发性跟腱断裂1例。
尿酸是一种常染色体隐性遗传病,由均质酸(HGA)氧化酶缺乏导致韧带、软骨、皮肤及各脏器中均质酸(HGA)产物积累引起。在这篇文章中,我们报告了一位61岁的男性患者,由于诊断为自发性跟腱断裂而手术,并根据术中组织的颜色和随后的检查诊断为尿酸尿。我们也回顾了尿酸及其伴随的病理根据文献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.90
自引率
43.80%
发文量
0
审稿时长
>12 weeks
期刊介绍: Joint Diseases and Related Surgery (formerly published as Eklem Hastalıkları ve Cerrahisi) is the official publication of the Turkish Joint Diseases Foundation. Joint Diseases and Related Surgery is open access journal. The full text of the articles of the Journal is freely available without embargo since 1990. Joint Diseases and Related Surgery is international, double-blind peer-reviewed periodical journal bringing the latest developments in all aspects of joint diseases and related surgey.
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