Related Experiment Video
Updated: Aug 20, 2026

Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry
Published on: November 5, 2019
[Acute complications in sickle cell disease]
Anoosha Habibi1, Dora Bachir, Bertrand Godeau
1Service de médecine interne, unité des maladies génétiques du globule rouge et d'aphérèse, CHU Henri Mondor, 94010 Créteil. anoosha.habibi@hmn.ap-hop-paris.fr
Abstract:
Sickle cell disease is an inherited disease characterised by the presence of an abnormal haemoglobin. Sickle cell disease can be complicated by acute vaso-occlusive crisis, which are the major clinical problem prompting admission to hospital and the major cause of death. It mainly manifests by osteo-articular pain and acute chest syndrome and can be complicated by multi-organ failure. The main treatment of severe acute vaso-occlusive crisis is based on transfusion.
Related Concept Videos
Complications of Diabetes Mellitus
Hemodialysis II: Procedure and Complications
Chronic Kidney Disease II: Clinical Manifestations
Acute Pancreatitis II: Pathophysiology
Peritoneal Dialysis II: Peritoneal Dialysis Systems and Complications
Hemorrhagic Stroke ll: Pathophysiology
