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  5. Follow up of Turkish and Syrian Thalassemic Patients in Gaziantep Region/Turkey-Struggling with pati

Follow up of Turkish and Syrian Thalassemic Patients in Gaziantep Region/Turkey-Struggling with pati

来源 :The 35th World Congress of the International Society of Hema | 被引量 : 0次 | 上传用户：hey_yuan
【摘 要】
：
Introduction Thalassemias are a heterogeneous group of autosomal recessive disorders that are characterized by hypochromic microcytic anemia caused by disturbed synthesis of one or more hemoglobin cha
【作 者】
：
Burcu Belen 
【机 构】
：
gaziantep childrens hospital
【出 处】
：
The 35th World Congress of the International Society of Hema
【发表日期】
：
2014年5期
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Introduction Thalassemias are a heterogeneous group of autosomal recessive disorders that are characterized by hypochromic microcytic anemia caused by disturbed synthesis of one or more hemoglobin chains.There are 1.300.000 beta thalassemia carriers and about 4000 beta thalassemia patients in Turkey.
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