Category: Medicine

What is Deficiency Factor XI? The disease was first described in 1953 by Rosenthal scientists and co-authors. Since 1962, according to the International Nomenclature, this factor is denoted by the number XI. Inheritance The disease

What is Hereditary Elliptocytosis? Hereditary elliptocytosis (synonym – ovalocytosis) is a hereditary deterministic disease transmitted by an autosomal dominant mode of inheritance. The erythrocyte anomaly that develops is characterized by a disorder of the structure

The main method of pathogenetic therapy and prevention of thromboembolism in thrombophilia is AT III replacement. If the patient has already received intensive heparin therapy, which is ineffective due to a deficiency of AT III,

What is Partial Red Cell Aplasia? Partial red cell aplasia (PRCA) is a syndrome with a sharp suppression of red blood cell production, isolated normochromic anemia, and deep reticulocytopenia. For the first time, PRCA described

What is Verlgof’s Disease? Thrombocytopenic purpura is a disease that develops against the background of an increased tendency of platelets to aggregate (“gluing”), manifested by the widespread formation of microthrombus, leading to blockage of the

What is Cytostatic Disease? Cytostatic disease is a kind of polysyndromic disease that occurs in connection with the action of cytostatic factors on the body and is characterized by the death of cells in the

What is Autoimmune Hemolytic Anemia? Under the name hemolytic anemia, a group of acquired and hereditary diseases is combined, characterized by increased intracellular or intravascular destruction of red blood cells. Autoimmune hemolytic anemia includes forms

What is Fanconi Anemia? The disease was described by Fankoni in 1927 in 3 children in the same family. Since that time, many family cases have been described. Causes of Fanconi Anemia Inheritance of the

What is Chronic Lymphocytic Leukemia? Chronic lymphocytic leukemia / small cell lymphocytic lymphoma (CLL / MLL), according to the WHO classification of tumor diseases of the hematopoietic and lymphoid tissues, is a tumor of monomorphic

What is Thalassemia? Under the thalassemia understand a group of hereditary diseases, manifested by a violation of the synthesis of any of the globin chains. With this form of pathology, hypochromic anemia is noted with