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Correlation of Transfusion Dependence and Its Associated Sequelae to Hematological and Biochemical Parameters in Patients With Sickle Cell Disease and Beta Thalassemia Major in Khobar: A Retrospective Study

Sickle cell disease (SCD) and beta thalassemia major (βTM) are multisystemic, genetically inherited diseases. They are caused by mutations of hemoglobin, which ultimately cause abnormal functioning of the red blood cells. The morbidity and mortality rates of these diseases are significant, as they m...

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Detalles Bibliográficos
Autores principales: Albahout, Khaled S, Yunus, Mohammed, Mohammad, Yaser G, Almalki, Adnan F, Alduailej, Saleh K, Alanazi, Basel Z
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10438923/
https://www.ncbi.nlm.nih.gov/pubmed/37602131
http://dx.doi.org/10.7759/cureus.42151