Hemoglobinopathies which comprise thalassemia along with sickle-cell anemia have been reported to have widespread. Approximately 5% of the global population is found to possess genes that are responsible for various hemoglobinopathies. The defect causes alteration in hemoglobin synthesis manifesting in variable degrees of anemia that ranges from clinical alterations those threatening to life. This hereditary type of anemia is the result of mutations in chromosome 16 that encodes globin genes and chromosome 11 encoding ϒ, δ, and β-globin. Hence; we presented the case report of a patient with Beta-Thalassemia Minor who underwent dental implant therapy

Dental Implant, Thalassemia