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Hemoglobin D (Hb D Punjab/ Los Angeles and Hb D Iran) and Co-Inheritance with Alpha- and Beta-Thalassemia in southern Iran
Hemoglobin (Hb) D Punjab Hb D Iran Hb D- beta- thalassemia (thal) Hb D-alpha- thal-1 trait Hb DSickle cell anemia
2015/9/23
Background: Hemoglobin-D (Hb D) is an uncommon structural hemoglobin variant, which is reported to be prevalent in north western India. There are only a few small series, of this entity in the literat...
Serum Folate Level Determination in Major Beta Thalassemia Patients
Beta major thalassemia Folic acid Hemoglobin Folate Trace elements
2009/12/14
Objective: Beta major thalassemia is a variant of beta thalassemia syndrome which could be treated with bone marrow transplantation or if not available, regular blood transfusion. In the later group, ...