2016 Introduction: Sickle cell disease (SCD) is a disorder caused by single gene mutation
and has systemic manifestations which include chronic hemolytic anemia, vaso-occlusive …

Sickle cell disease is the most common inherited haemoglobinopathy described.
Complications of sickle cell disease (SCD) are due to chronic haemolysis of fragile red cells …

Sickle cell disease (SCD), one of the most common inherited genetic syndromes in the USA,
is characterized by recurring episodes of acute illness and progressive multisystem organ …

Sickle cell disease is an inherited hemolytic disease with systemic complications. These
complications significantly impact the patients' quality of life. There are characteristic …

Sickle cell anemia-a review of the imaging findings LEARNING OBJECTIVES: To review and
describe the manifestations of sickle cell anemia, focusing on the typical imaging findings in …

At least 25% of individuals with sickle cell disease will have a neurological complication
over their lifetime, often as early as in childhood. Neuroradiological findings in patients with …

Sickle cell disease is the most common hereditary hemoglobinopathy, which results in
abnormally shaped and rigid red blood cells. These sickle‐shaped red blood cells cause …

Sickle cell disease results from the presence of abnormal β globin chains within hemoglobin
and may be manifested in anemia, vaso-occlusion, and superimposed infection. The gene …

Sickle cell disease (SCD) is an autosomal recessive haemoglobinopathy, which manifests
as multisystem ischaemia and infarction, as well as haemolytic anaemia. The morphological …

Introduction: Over the past decades, neuroimaging studies have clarified that a significant
proportion of patients with sickle cell disease (SCD) have functionally significant brain …