We describe rare cases of heterozygous complex mutations in the form of SEA-HPFH and β –thalassemia. This discovery allows the development of a prenatal diagnostic test for families carrying this mutation in subsequent pregnancies.

Thalassemia is a hereditary blood disorder characterized by reduced hemoglobin levels in the body. Asides from medical treatment, the following article will convey how proper nutrition plays a crucial role in improving patients’ hemoglobin levels.