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Heart Involvement in Hemoglobinopathies: Two Case Reports and Brief Review of Literature
Abstract
Wael Yaakoubi, Manel Ben Hlima, Sana Ouali, Fathia Mghaith, Med Sami Mourali
Hereditary haemoglobin disorders, also termed haemoglobinopathies, include mainly beta-thalassemia and sickle cell disease and represent the most common monogenic disorders in human. Cardiac complications are still a leading cause of mortality and morbidity in patients with haemoglobinopathy, have dramatically reduced in patient populations receiving modern regular therapy and follow-up.