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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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Opportunities to Improve Outcomes in Sickle Cell Disease
Opportunities to Improve Outcomes in Sickle Cell Disease
Sickle cell ulcers
American Family Physician
American Family Physician
American Family Physician

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
Myocardial ischaemia in children with sickle cell disease
American Journal of Roentgenology
American Journal of Roentgenology
Archives of Disease in Childhood

Acute Lymphoblastic Leukemia in Sickle Cell Disease
Chronic Myelogenous Leukemia in Sickle Cell Anemia
Pulmonary Thrombotic Arteriopathy in Patients With Sickle Cell Disease
Archives of Pathology and Laboratory Medicine
Archives of Pathology and Laboratory Medicine
Archives of Pathology and Laboratory Medicine

Pulmonary Thrombotic Arteriopathy in Patients With Sickle Cell Disease
The Placenta in Sickle Cell Disease
Aplastic Crisis in a Patient with Sickle Cell Disease
Archives of Pathology and Laboratory Medicine
Archives of Pathology and Laboratory Medicine
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

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Php programming by Robert Barbey  
Edited by Aldo Campana, November 3, 2009