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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Detalles Bibliográficos
Autores principales: Shaikh, Ashraf, Desai, Mohan, Kantanavar, Radhakrishna, Shah, Swapneel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933647/
https://www.ncbi.nlm.nih.gov/pubmed/33708713
http://dx.doi.org/10.13107/jocr.2020.v10.i08.1860

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933647/
https://www.ncbi.nlm.nih.gov/pubmed/33708713
http://dx.doi.org/10.13107/jocr.2020.v10.i08.1860

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