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Hematology. Hematologic diseases are disorders which primarily affect the blood and blood-forming organs. Hematologic diseases include rare genetic disorders, anemia, HIV, sickle cell disease and complications from chemotherapy or transfusions.
Beta-thalassemia (β-thalassemia) is an autosomal dominant blood condition that results in the reduction of hemoglobin production. The cause for the disorder is related to a genetic mutation of the HBB gene. This gene is responsible for providing the instructions to produce beta-globin; one of the major components of hemoglobin.
Immune thrombocytopenic purpura ( ITP ), also known as idiopathic thrombocytopenic purpura or immune thrombocytopenia, is an autoimmune primary disorder of hemostasis characterized by a low platelet count in the absence of other causes. [ 1][ 2] ITP often results in an increased risk of bleeding from mucosal surfaces (such as the nose or gums ...
Thrombotic thrombocytopenic purpura ( TTP) is a blood disorder that results in blood clots forming in small blood vessels throughout the body. [ 2] This results in a low platelet count, low red blood cells due to their breakdown, and often kidney, heart, and brain dysfunction. [ 1] Symptoms may include large bruises, fever, weakness, shortness ...
Anemia or anaemia ( British English) is a blood disorder in which the blood has a reduced ability to carry oxygen. This can be due to a lower than normal number of red blood cells, a reduction in the amount of hemoglobin available for oxygen transport, or abnormalities in hemoglobin that impair its function. [ 3][ 4]
Thalassemias are inherited blood disorders that result in abnormal hemoglobin. [ 7] Symptoms depend on the type of thalassemia and can vary from none to severe. [ 1] Often there is mild to severe anemia (low red blood cells or hemoglobin) as thalassemia can affect the production of red blood cells and also affect how long the red blood cells ...
In hematology, essential thrombocythemia ( ET) is a rare chronic blood cancer ( myeloproliferative neoplasm) characterised by the overproduction of platelets (thrombocytes) by megakaryocytes in the bone marrow. [ 3] It may, albeit rarely, develop into acute myeloid leukemia or myelofibrosis. [ 3] It is one of the blood cancers wherein the bone ...
This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes D50-D89 within Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism should be included in this category.
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