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Hematology

Hematology

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Antiphospholipid syndrome What we need to know
Antiphospholipid syndrome What we need to know

Etiology Antiphospholipid syndrome is an autoimmune disease. Symptoms and clinical manifestations are diverse, of which arterial and venous ...

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Aplastic anemia What we need to know
Aplastic anemia What we need to know

Aplastic anemia is a rare and very serious blood disorder. It is caused by bone marrow damage, which...

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Genetic thrombophilia What we need to know
Genetic thrombophilia What we need to know

Thrombophilia is a condition in which the probability of blood clots is increased. This condition is called hypercoagulation. Thrombophilia may be...

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Thalassemia What we need to know
Thalassemia What we need to know

Thalassemia belongs to the group of hereditary hemolytic anemias. Hemolytic anemias are a large group of diseases that differ from each other in reasons, clinical...

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Sickle cell anemia What we need to know
Sickle cell anemia What we need to know

Sickle cell anemia is a hereditary disease in which the red blood cells have a sickle (crescent) shape and their...

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Pernicious (B12 deficiency) anemia What we need to know
Pernicious (B12 deficiency) anemia What we need to know

  Same as: Biermer's Disease Pernicious anemia is a condition developed as a result of vitamin B12 deficiency. …

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Factor XI deficiency What we need to know
Factor XI deficiency What we need to know

"Factor XI deficiency" is a pathology in which the blood clotting process is disturbed. As a result, having this disease...

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Von Willebrand's disease What we need to know
Von Willebrand's disease What we need to know

About the disease Von Willebrand factor is a protein involved in blood clotting, which ensures the primary adhesion of platelets...

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