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Acute Intermittent Porphyria

26.07.2019 blood-pressure-meds Diseases

What is Acute Intermittent Porphyria? Acute intermittent porphyria is a genetically determined disease caused by damage to the central nervous system, less commonly the peripheral nervous system, recurrent abdominal pain, increased blood pressure and pink

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Hereditary Stomatocytosis

19.07.2019 blood-pressure-meds Diseases

What is Hereditary Stomatocytosis? Hereditary stomatocytosis is a hereditarily deterministic disease transmitted by an autosomal dominant mode of inheritance. In this disease, the inherited erythrocyte abnormality is caused by a defect in the erythrocyte membrane

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Hereditary Factor X Deficiency

12.07.2019 blood-pressure-meds Diseases

What is Hereditary Factor X Deficiency? The existence of factor X and its hereditary deficiency was first proved by the scientist Telfer, as well as the co-authors in 1956 Stewart’s disease – Prouer – a

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Hereditary Megaloblastic Anemia in Lesch-Nayan Syndrome

05.07.2019 blood-pressure-meds Diseases

What is Hereditary Megaloblastic Anemia for Lesch-Nayan Syndrome? Lesch-Nyana syndrome is a rare inherited disorder. Hereditary megaloblastic anemia in Rogers syndrome. For the first time in 1969, Rogers and co-authors described a complex hereditary syndrome

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The Mechanism of Inhibition of Normal Blood Formation in Hemoblastosis

21.06.2019 blood-pressure-meds Diseases

What is The Mechanism of Inhibition of Normal Blood Formation in Hemoblastosis? In itself, the suppression of normal hematopoiesis in tumors of hematopoietic cells is the main link in their developmental mechanism. There is no

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Immune Hemolytic Anemia

31.05.2019 blood-pressure-meds Diseases

What is Immune Hemolytic Anemia? Immune hemolytic anemia is a large heterogeneous group of diseases for which the participation of antibodies or immune lymphocytes in the damage and premature death of erythrocytes or erythrocaryocytes is

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Factor XII Deficiency

24.05.2019 blood-pressure-meds Diseases

What is Factor XII Deficiency? This disease is considered to be a rather rare violation of coagulation hemostasis. For the first time pathology was revealed by O. Ratnov in 1964. The disease is characterized by

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Factor V Deficiency

17.05.2019 blood-pressure-meds Diseases

What is Deficiency Factor V? For the first time, a patient with a hereditary coagulation factor deficiency was described in 1947. Subsequently, this factor received the following designations: labile factor, proaccelerin, Ac-globulin, factor V. Factor

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