Does Your Patient’s Urine Turns Dark? Alkaptonuria and Low Back Ache: A Literature Review

INTRODUCTION: Alkaptonuria is a very rare inborn error of amino acid metabolism due to deficient homogentisic acid (HGA) oxidase enzyme leading to accumulation of HGA in plasma, cartilage, other tissues of human body and its excretion in urine. It has both systemic and peripheral signs and symptoms....

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Detalles Bibliográficos
Autores principales: Kanniyan, Kalaivanan, Pathak, Aditya C, Dhammi, Ish Kumar, Jain, Anil Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4719265/
https://www.ncbi.nlm.nih.gov/pubmed/27298997
http://dx.doi.org/10.13107/jocr.2250-0685.220

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4719265/
https://www.ncbi.nlm.nih.gov/pubmed/27298997
http://dx.doi.org/10.13107/jocr.2250-0685.220

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