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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