Ochronotic Surprise during Total Knee Replacement! A Case Report

INTRODUCTION: Alkaptonuria is a rare autosomal recessive metabolic disorder characterized by accumulation of homogentisic acid (HGA) due to an inherited deficiency of the enzyme HGA oxidase. Unlike rheumatoid arthritis which affects the small joints of the hands and feet, ochronotic arthropathy pred...

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Detalles Bibliográficos
Autores principales: G, Syam, John, John Thayyil, Nair, Dileep Sasidharan, Yadav, Shikhar, Varghese, Joice, T, Jamsheed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930298/
https://www.ncbi.nlm.nih.gov/pubmed/35415103
http://dx.doi.org/10.13107/jocr.2021.v11.i10.2464

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930298/
https://www.ncbi.nlm.nih.gov/pubmed/35415103
http://dx.doi.org/10.13107/jocr.2021.v11.i10.2464

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