Cerebral hemodynamic in patients with major β-Thalassemia using transcranial Doppler sonography

نویسندگان
Iranmanesh, Farhad ID 1
Dehesh, Tania ID 2
Abutorabi-zarchi, Marzieh ID 3
Hashemi, Azam ID 4
Jenabzade, Alireza ID 5
Akhavanghalibaf, Mahvash ID 6

1 Neurology Research Center, Kerman University of Medical Sciences, Kerman, Iran

2 Department of Biostatistics and Epidemiology, Kerman University of Medical Sciences, Kerman.

3 Shahid Sadoughi University of Medical Sciences, Yazd, Iran

4 Hematology and Oncology research center , Shahid Sadoughi University of Medical Sciences, Yazd, Iran

5 Hematology and Oncology research center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran

6 Hematology and Oncology Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran

doi
10.18502/ijpho.v11i3.6566
چکیده

Background: β-thalassemia, a severe form of anemia, is an inherited blood disorder characterized by growth retardation, splenomegaly, and bone abnormalities. Complications related to treatment-induced iron overload also affect the quality of life of patients with major β-thalassemia. Some recent studies indicated cerebral hemodynamic disorders and increased risk of stroke in these ...

کلیدواژه‌ها
Major thalassemia, Cerebral, Hemodynamic