Sickle cell anemia

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Sickle cell anemia

Anemia, sickle cell

Hemoglobin S disease

Sickle cell disease

[Clinical features: sickle-shaped red blood cells; chronic hemolytic anemia; vaso-occlusive crises resulting in ischemia, painful episodes, and multiple organ damage]

[Inheritance: autosomal recessive]

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40-year-old man with sickle cell disease and frequently recurring painful crises who presented with abdominal pain	40-year-old man with sickle cell disease and frequently recurring painful crises who presented with abdominal pain	Renal Doppler Indices in Sickle Cell Disease: Early Radiologic Predictors of Renovascular Changes
American Journal of Roentgenology	American Journal of Roentgenology	American Journal of Roentgenology


Renal Doppler Indices in Sickle Cell Disease: Early Radiologic Predictors of Renovascular Changes	Myocardial ischaemia in children with sickle cell disease	Aplastic Crisis in a Patient with Sickle Cell Disease
American Journal of Roentgenology	Archives of Disease in Childhood	ASH Image Bank


Aplastic Crisis in a Patient with Sickle Cell Disease	Aplastic Crisis in a Patient with Sickle Cell Disease	Aplastic Crisis in a Patient with Sickle Cell Disease
ASH Image Bank	ASH Image Bank	ASH Image Bank


Aplastic Crisis in a Patient with Sickle Cell Disease	Aplastic Crisis in a Patient with Sickle Cell Disease	Aplastic Crisis in a Patient with Sickle Cell Disease
ASH Image Bank	ASH Image Bank	ASH Image Bank


Pappenheimer Bodies in Sickle Cell Disease	Pappenheimer Bodies in Sickle Cell Disease	Pappenheimer Bodies in Sickle Cell Disease
ASH Image Bank	ASH Image Bank	ASH Image Bank

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Edited by Aldo Campana, February 8, 2010