Noun:

थॅलेसेमिया,

thalassemias's Usage Examples:

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.

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

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

Diseases such as beta thalassemias, which affect components of the adult hemoglobin, can delay this process.

Congenital dyserythropoietic anemia (CDA) is a rare blood disorder, similar to the thalassemias.

deficiency shows anisocytosis, anisochromia and elliptocytosis, and thalassemias demonstrate target cells and coarse basophilic stippling.

elliptocytosis, and thalassemias demonstrate target cells and coarse basophilic stippling.

is usually harmless unlike other hemoglobin variants such as HbS and thalassemias, even under combination with these abnormal hemoglobins.

Anemia of chronic disease shows unremarkable RBCs, iron deficiency shows anisocytosis, anisochromia and elliptocytosis, and thalassemias demonstrate target cells and coarse basophilic stippling.

Alpha thalassemias result from deletions of each of the alpha genes as well as deletions of both HBA2 and HBA1; some nondeletion alpha thalassemias have.

Thus, some hemoglobinopathies are also thalassemias, but most are not.