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Spontaneous Achilles tendon rupture in alkaptonuria
Alkaptonuria (AKU) is a rare inborn metabolic disease characterized by accumulation of homogentisic acid (HGA). Excretion of HGA in urine causes darkening of urine and its deposition in connective tissues causes dark pigmentation (ochronosis), early degeneration of articular cartilage, weakening of...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Saudi Medical Journal
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707406/ https://www.ncbi.nlm.nih.gov/pubmed/26620992 http://dx.doi.org/10.15537/smj.2015.12.12834 |
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author | Alajoulin, Omar A. Alsbou, Mohammed S. Ja’afreh, Somayya O. Kalbouneh, Heba M. |
author_facet | Alajoulin, Omar A. Alsbou, Mohammed S. Ja’afreh, Somayya O. Kalbouneh, Heba M. |
author_sort | Alajoulin, Omar A. |
collection | PubMed |
description | Alkaptonuria (AKU) is a rare inborn metabolic disease characterized by accumulation of homogentisic acid (HGA). Excretion of HGA in urine causes darkening of urine and its deposition in connective tissues causes dark pigmentation (ochronosis), early degeneration of articular cartilage, weakening of the tendons, and subsequent rupture. In this case report, we present a rare case of a patient presented with unilateral spontaneous rupture of Achilles tendon due to AKU. The patient developed most of the orthopedic manifestations of the disease earlier than typical presentations. Alkaptonuria patients should avoid strenuous exercises and foot straining especially in patients developing early orthopedic manifestations. |
format | Online Article Text |
id | pubmed-4707406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Saudi Medical Journal |
record_format | MEDLINE/PubMed |
spelling | pubmed-47074062016-01-21 Spontaneous Achilles tendon rupture in alkaptonuria Alajoulin, Omar A. Alsbou, Mohammed S. Ja’afreh, Somayya O. Kalbouneh, Heba M. Saudi Med J Case Report Alkaptonuria (AKU) is a rare inborn metabolic disease characterized by accumulation of homogentisic acid (HGA). Excretion of HGA in urine causes darkening of urine and its deposition in connective tissues causes dark pigmentation (ochronosis), early degeneration of articular cartilage, weakening of the tendons, and subsequent rupture. In this case report, we present a rare case of a patient presented with unilateral spontaneous rupture of Achilles tendon due to AKU. The patient developed most of the orthopedic manifestations of the disease earlier than typical presentations. Alkaptonuria patients should avoid strenuous exercises and foot straining especially in patients developing early orthopedic manifestations. Saudi Medical Journal 2015-12 /pmc/articles/PMC4707406/ /pubmed/26620992 http://dx.doi.org/10.15537/smj.2015.12.12834 Text en Copyright: © Saudi Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Alajoulin, Omar A. Alsbou, Mohammed S. Ja’afreh, Somayya O. Kalbouneh, Heba M. Spontaneous Achilles tendon rupture in alkaptonuria |
title | Spontaneous Achilles tendon rupture in alkaptonuria |
title_full | Spontaneous Achilles tendon rupture in alkaptonuria |
title_fullStr | Spontaneous Achilles tendon rupture in alkaptonuria |
title_full_unstemmed | Spontaneous Achilles tendon rupture in alkaptonuria |
title_short | Spontaneous Achilles tendon rupture in alkaptonuria |
title_sort | spontaneous achilles tendon rupture in alkaptonuria |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707406/ https://www.ncbi.nlm.nih.gov/pubmed/26620992 http://dx.doi.org/10.15537/smj.2015.12.12834 |
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