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Arthroscopic diagnosis and treatment of shoulder ochronotic arthropathy – A case report
Alkaptonuria is a rare inherited metabolic disorder, caused by the deficiency of homogentisate 1,2 dioxygenase enzyme. The three major features of alkaptonuria are the presence of homogentisic acid in urine, ochronosis (bluish-black pigmentation in connective tissue) and arthritis of the spine and l...
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| 發表在: | J Clin Orthop Trauma |
|---|---|
| Main Authors: | , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Elsevier
2017
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5574846/ https://ncbi.nlm.nih.gov/pubmed/28878548 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jcot.2016.11.009 |
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