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Medical Term:

thalassemia intermedia


Definition: a clinical variant of thalassemia characterized by an intermediate degree of severity. These patients have severe anemia but usually do not require regular blood transfusions. Intermedia disorders represent a heterogeneous group of genetic disorders and may include cases with homozygous or heterozygous abnormalities in the ß-globin chain gene.

© Copyright 2016 Wolters Kluwer. All Rights Reserved. Review Date: Sep 19, 2016.