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Updated: Aug 8, 2026

Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
Sickle cell hemoglobin C disease in Saudi Arabia
Zakaria M Al-Hawsawi1, Mohammed S Islam, Nabil S Shehata
1Department of Pediatrics, Madinah Maternity & Children's Hospital, PO Box 6205, Madinah Al-Munawara, Kingdom of Saudi Arabia. zhawsawi@yahoo.com.
Abstract:
Sickle cell hemoglobin C (HbSC) is a disease confined to people of West African ancestry and it has not been reported in the Kingdom of Saudi Arabia (KSA). We are reporting 2 patients with HbSC disease from the western province of KSA (Madinah); one patient presented with severe form of the disease which include transient hypertension.
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