Syncope Following Treatment of UTI: A Case of Acute Hemolytic Anemia, Methemoglobinemia and Acute Renal Dysfunction Following Phenazopyridine Use in a Patient With G6PD Deficiency

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked recessive genetic disorder which commonly affects males. It is due to a defect in the red blood cell enzyme, G6PD. Lack of G6PD makes the RBCs vulnerable to oxidant stress resulting in hemolysis. The severity of hemolytic anemia vari...

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Detalles Bibliográficos
Autores principales: Khan, Omair, Uddin, Syed M.M., Atuaka, Christiana, Farooqui, Arafat A., Maheshwari, Sanjay, Zaw, Thi H., Tabba, Jude, Seitllari, Armando, Maharaj, Sime, Khan, Muhammad H., Seneviratne, Chanaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Greater Baltimore Medical Center 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9924616/
https://www.ncbi.nlm.nih.gov/pubmed/36817304
http://dx.doi.org/10.55729/2000-9666.1144

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9924616/
https://www.ncbi.nlm.nih.gov/pubmed/36817304
http://dx.doi.org/10.55729/2000-9666.1144

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