A Previously Undiagnosed Case of Alkaptonuria in an 80-Year-Old Patient: A Case Report

Alkaptonuria is a rare genetic metabolic disorder of autosomal recessive inheritance characterised by the accumulation of homogentisic acid in the body. It is diagnosed upon identification of characteristic symptoms, using various biochemical investigations, radiographic pictures, and a variety of s...

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Detalles Bibliográficos
Autores principales: Singh, Mohit K, Memon, Faisal A, Deokar, Smita A, Achhapalia, Yash, Yeotiwad, Ganesh R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10072848/
https://www.ncbi.nlm.nih.gov/pubmed/37025736
http://dx.doi.org/10.7759/cureus.35792

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10072848/
https://www.ncbi.nlm.nih.gov/pubmed/37025736
http://dx.doi.org/10.7759/cureus.35792

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