Incidental diagnosis of ochronosis by aortic valve replacement

Alkaptonuria is a rare inherited metabolic disease caused by homogentisic acid oxidase enzyme deficiency. Homogentisic acid formed during phenylalanine and tyrosine metabolism cannot be further metabolized and accumulates due to this enzyme deficiency. Some of the homogentisic acid that cannot be re...

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Detalles Bibliográficos
Autores principales: Çoban, Özgür, Uçak, Hacı Ali, Güldür, Muhammet Ahmet, Özsöyler, İbrahim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bayçınar Medical Publishing 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8990137/
https://www.ncbi.nlm.nih.gov/pubmed/35444851
http://dx.doi.org/10.5606/tgkdc.dergisi.2022.20909

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8990137/
https://www.ncbi.nlm.nih.gov/pubmed/35444851
http://dx.doi.org/10.5606/tgkdc.dergisi.2022.20909

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