A rare case of coinheritance of Hemoglobin H disease and sickle cell trait combined with severe iron deficiency
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We present a case of a 40-year-old female from Turkey, who was referred to our outpatient clinic for an undetermined thalassemia and sickle cell trait. At first consultation hemoglobin was decreased (71 g/L) with microcytosis (MCV 55.1 fL), and hypochromia (MC... ...
