Mortality and complications in Omani patients with beta-thalassemia major: a long-term follow-up study

BACKGROUND AND AIM: Beta thalassemia major (β-TM) is a genetic blood disorder requiring lifelong blood transfusions. The resulting iron overload damages multiple organs, particularly the heart and endocrine organs. This study aimed to describe and assess the predictors of survival and complications...

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Detalles Bibliográficos
Autores principales: Daar, Shahina, Al-Naamani, Khalid, de Sanctis, Vincenzo, Al Rahbi, Sarah, Zedjali, Shoaib, Khan, Hammad, Panjwani, Vinodh K, Al-Khabori, Murtadha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10440768/
https://www.ncbi.nlm.nih.gov/pubmed/37539594
http://dx.doi.org/10.23750/abm.v94i4.14856

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10440768/
https://www.ncbi.nlm.nih.gov/pubmed/37539594
http://dx.doi.org/10.23750/abm.v94i4.14856

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