Total Shoulder Reverse Arthroplasty in Alkaptonuria: An Effective Option to Treat a Complication of a Rare Disease

INTRODUCTION: Alkaptonuria (AKU) is a rare autosomal recessive disorder in which tyrosine metabolism is altered. There is a deficiency of the Homogentisate 1,2-dioxygenase enzyme (homogentisic acid oxidase) This enzyme is responsible for the metabolism of the tyrosine - homogentisic acid - in maleyl...

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Detalles Bibliográficos
Autores principales: Afonso, Carolina Tiago, Pinto, Susana, Freitas, Miguel, Pedrosa, Diana, Ruano, Afonso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9091386/
https://www.ncbi.nlm.nih.gov/pubmed/35611280
http://dx.doi.org/10.13107/jocr.2022.v12.i01.2604

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9091386/
https://www.ncbi.nlm.nih.gov/pubmed/35611280
http://dx.doi.org/10.13107/jocr.2022.v12.i01.2604

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