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A complete blood count (CBC), also known as a full blood count (FBC), is a set of medical laboratory tests that provide information about the cells in a person's blood.The CBC indicates the counts of white blood cells, red blood cells and platelets, the concentration of hemoglobin, and the hematocrit (the volume percentage of red blood cells).
Blood plasma volume may be expanded by or drained to extravascular fluid when there are changes in Starling forces across capillary walls. For example, when blood pressure drops in circulatory shock, Starling forces drive fluid into the interstitium, causing third spacing.
A complete blood type would describe each of the 45 blood groups, and an individual's blood type is one of many possible combinations of blood-group antigens. [3] Almost always, an individual has the same blood group for life, but very rarely an individual's blood type changes through addition or suppression of an antigen in infection, malignancy, or autoimmune disease.
Separating serum proteins by electrophoresis is a valuable diagnostic tool, as well as a way to monitor clinical progress.Current research regarding blood plasma proteins is centered on performing proteomics analyses of serum/plasma in the search for biomarkers.
One of King Abdulaziz's vehicles on display at the King Abdulaziz Memorial Hall, 2012. King Abdulaziz Foundation for Research and Archives (KAFRA) (Arabic: دارة الملك عبد العزيز), better known as Darah, [1] is a cultural institution in the Al Murabba neighborhood of Riyadh, Saudi Arabia, located between the Murabba Palace compound and the National Museum.
Hemoglobinopathies (congenital abnormality of the hemoglobin molecule or of the rate of hemoglobin synthesis) . Sickle cell disease; Thalassemia; Methemoglobinemia; Anemias (lack of red blood cells or hemoglobin)
Thalassemias are a group of inherited blood disorders that manifest as the production of reduced hemoglobin. [7] Symptoms depend on the type of thalassemia and can vary from none to severe, including death. [1]
Hypokalemic periodic paralysis (hypoKPP), also known as familial hypokalemic periodic paralysis (FHPP), [1] is a rare, autosomal dominant channelopathy characterized by muscle weakness or paralysis when there is a fall in potassium levels in the blood (hypokalemia).