
Thrombocytosis is a pathological increase in the number of platelets in the blood. Depending on the origin, primary and secondary thrombocytosis are distinguished. Primary, or
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Thrombocytosis is a pathological increase in the number of platelets in the blood. Depending on the origin, primary and secondary thrombocytosis are distinguished. Primary, or

Burkitt lymphoma is a rare but very aggressive B-cell non-Hodgkin lymphoma that most often affects children and adolescents.

Anemia is defined as a decrease in the number of red blood cells in the circulating blood. It is a widespread pathology in the population.

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

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

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

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

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

Multiple myeloma Multiple myeloma belongs to a group of blood cancers that form from plasma cells. Healthy plasma

Factor XI deficiency (hemophilia C) is a rare inherited blood clotting disorder that usually causes modest