Complications of Transfusion-Dependent β-Thalassemia Patients in Sistan and Baluchistan, South-East of Iran

Complications of Transfusion-Dependent β-Thalassemia Patients in Sistan and Baluchistan, South-East of Iran

Background:Thalassemia syndromes are among prevalent hereditary disorders imposing high expenses on health-care system worldwide and in Iran. Organ failure represents a life-threatening challenge in transfusion- dependent β-thalassemia (TDT) patients. The purpose of the present study was to determin...

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Autori principali: Maryam Yaghobi, Ebrahim Miri-Moghaddam, Majid Naderi, Ali Bazi, Ali Navidian, Asiyeh Kalkali
Natura: Articolo
Lingua:English
Pubblicazione: Tehran University of Medical Sciences 2017-10-01
Serie:International Journal of Hematology-Oncology and Stem Cell Research
Soggetti:
β- thalassemia major
Iron overload
Organ dysfunction
Cardiac disease
Accesso online:https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/681

Accesso online

https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/681

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