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Updated: Aug 12, 2026

Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
[Clinical development of beta-thalassemia-sickle cell anemia apropos of 36 cases]
I Thuret1, G Michel, D Lena-Russo
1Service de pédiatrie et d'hématologie pédiatrique, hôpital d'enfants de La Timone, Marseille, France.
Abstract:
Hematological and clinical features of 36 mainly Algerian patients with S-beta thalassemia are reported. These data, compared with those reported in the literature, showed a higher prevalence of aseptic necrosis and gall stones, probably related to the large predominance of S-beta zero-thalassemia (30 cases) and a long (14 years) median follow-up period.
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