Author: blood-pressure-meds

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

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

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

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

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

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

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

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