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Intraoperative Diagnosis of a Rare Case of Arthropathy – A Case Report and Review of Literature
INTRODUCTION: Alkaptonuria is a rare metabolic disorder of autosomal recessive pattern of inheritance caused due to homogentisic acid oxidase enzyme deficiency. As a result, polymers of homogentisic acid get deposited in excessive amounts in the connective tissues, leading to brownish-black pigmenta...
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| Vydáno v: | J Orthop Case Rep |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Indian Orthopaedic Research Group
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7933647/ https://ncbi.nlm.nih.gov/pubmed/33708713 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.13107/jocr.2020.v10.i08.1860 |
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