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Meaning h: hr / hours H: histamine or its receptors (if with subscripts) hemagglutinin: H x: history: HA ; H/A hypertonia arterialis headache calcium hydroxyapatite HAA: hepatitis-associated antigen or #History As Above HAART: highly active antiretroviral therapy HACA: human anti-chimeric antibody: HACE: High-altitude cerebral edema: HACEK
Hyperhomocysteinemia is a medical condition characterized by an abnormally high level of total homocysteine (that is, including homocystine and homocysteine-cysteine disulfide) in the blood, conventionally described as above 15 μmol/L. [1]
High levels of homocysteine in the blood (hyperhomocysteinemia) is regarded as a marker of cardiovascular disease, likely working through atherogenesis, which can result in ischemic injury. Therefore, hyperhomocysteinemia is a possible risk factor for coronary artery disease .
Polycythemia (also known as polycythaemia) is a laboratory finding in which the hematocrit (the volume percentage of red blood cells in the blood) and/or hemoglobin concentration are increased in the blood.
Hematocrit levels that are too high or too low can indicate a blood disorder, dehydration, or other medical conditions. [4] An abnormally low hematocrit may suggest anemia, a decrease in the total amount of red blood cells, while an abnormally high hematocrit is called polycythemia. [5] Both are potentially life-threatening disorders.
Deficiencies of Vitamin B 12 or folate produce a macrocytic anemia (large cell anemia) in which the RDW is elevated in roughly two-thirds of all cases. However, a varied size distribution of red blood cells is a hallmark of iron deficiency anemia, and as such shows an increased RDW in virtually all cases.
Extremely high levels of unconjugated bilirubin in plasma enables bilirubin to cross the blood-brain-barrier to reach the brain and central nervous system to impart damage. This is termed kernicterus, or bilirubin encephalopathy. Kernicterus is rare in adults but is prevalent in newborns with underdeveloped blood-brain barriers and lower ...
Hemoglobin analysis, with tests such as high-performance liquid chromatography, along with genetic testing are required for the confirmation of Hb H disease. [ 6 ] [ 7 ] Patients may also laboratory abnormalities indicative of low red blood cells, including changes in hemoglobin, red cell distribution width , hematocrit , mean corpuscular ...