Final answer:
The total number of genes involved in α-thalassemia due to a three gene deletion is 4. When there is a deletion of three genes, it leads to the formation of abnormal hemoglobin called HbH, which is associated with severe anemia.
Step-by-step explanation:
The total number of genes involved in α-thalassemia due to a three gene deletion is 4.
In alpha-thalassemia, there are four genes that play a role in the synthesis of the α-chain of globin. These genes are usually present in pairs, and when there is a deletion of three genes, it leads to the formation of abnormal hemoglobin called HbH.
HbH disease is characterized by severe anemia and a decrease in the levels of hemoglobin. The lack of α-chain results in the formation of different combinations of β and γ chains, leading to impaired transport of oxygen by Hb.