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Thrombocytopenia 4
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1. Anti-phospholipid syndrome Anti-phospholipid syndrome is an autosomally inherited genetic disorder in which an affected individual produces antibodies against his/her own cellular phospholipid components. This is manifested clinically as a tendency to have arterial and venous thrombosis , thrombocytopenia and recurrent fetal loss (miscarriage).
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2. Hemolytic uremic syndrome Hemolytic uremic syndrome is characterized by microangiopathic hemolytic anemia, thrombocytopenia, and kidney failure (decreased glomerular filtration, protein and blood in the urine).
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3. Thrombocytopenia thrombocytopenia is a condition in which the patient's platelet count in the blood is less than normal (150 - 400 109 per liter)
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4. Wiskott-Aldrich syndrome Wiskott-Aldrich syndrome is characterized by thrombocytopenia, eczema, and infection prone because of immunodeficiency. Inheritance is X-linked recessive.
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