Unit Objectives - 2

Unit objectives:

5. List the thalassemias associated with genetic defects of the beta gene cluster and describe the clinical expression of each heterozygous and homozygous form.

6. Describe laboratory findings in heterozygous and homozygous b- thalassemias.

7. Describe the treatment of homozygous b-thalassemia, and the risks involved, and list the laboratory tests used to monitor iron levels.