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β-thalassemia intermedia (TI) patients can present with a severe clinical disease at 2–6 years of age or remain asymptomatic until adult life. They suffer from mild anemia (hemoglobin (Hb) between 7–10 g/dL), and are usually transfusion independent.[1][1] Pregnancy in these women, whether

Pregnancy outcome in patients with -thalassemia intermedia at two tertiary care centers, in Beirut and Milan