Article ID Journal Published Year Pages File Type
3984295 Clinical Radiology 2007 11 Pages PDF
Abstract

Sickle cell disease (SCD) is an inherited abnormality of the ß-globin chain, which causes a spectrum of haemolytic anaemias. Clinical manifestations in SCD include anaemia, jaundice, recurrent vaso-occlusive crises, and infections (particularly by encapsulated bacteria) due to functional asplenia and cerebrovascular accidents. Radiological investigations play a critical role both in the diagnosis and in the primary prevention of the complications of SCD.

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