హేమోగ్లోబిన్ యొక్క తప్పు సంశ్లేషణ కారణంగా రక్తహీనత యొక్క వారసత్వ రూపం,

Noun:

తలన్రేలు చేయు,

thalassemia's Usage Examples:

Kreger et al combining a retrospective review of three cases of alpha thalassemia major and a literature review of 17 cases found that in utero transfusion.

any normal form of hemoglobin, as in the group of diseases known as thalassemias.

whose group was at the time establishing the molecular bases of the thalassemias, he returned to Brazil and started a research group with a major scientific.

as HbS and thalassemias, even under combination with these abnormal hemoglobins.

endocrine organs, in patients who receive or did receive frequent blood transfusions (such as those with thalassemia, sickle cell disease, leukemia, aplastic.

Beta-thalassemia major is an inherited blood disease in which.

particular, a group of inherited haematological disorders known as the thalassemias that are associated with abnormalities in the production of globin, the.

α-thalassemia is mostly found in sub-tropical.

Pathologic EMH can be caused by myelofibrosis, thalassemias or disorders caused in the hematopoietic system.

Alpha-thalassemia (α-thalassemia, α-thalassaemia) is a form of thalassemia involving the genes HBA1 and HBA2.

In practice though elliptocytes and anisocytosis are often seen in thalassemia and target cells occasionally in iron deficiency.

attributed to various anemias, most often; beta thalassemia major, a form of microcytic anemia.

Conditions such as infectious mononucleosis, thalassemia, and cirrhotic liver disease may all involve splenomegaly.