Fathia Mghaith
La Rabta Hospital, Ministry of Public Health, Tunisia
Publications
-
Case Report
Heart Involvement in Hemoglobinopathies: Two Case Reports and Brief Review of Literature
Author(s): Wael Yaakoubi*, Manel Ben Hlima, Sana Ouali, Fathia Mghaith and 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... Read More»