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  2. Haptoglobin - Wikipedia

    en.wikipedia.org/wiki/Haptoglobin

    Haptoglobin (abbreviated as Hp) is the protein that in humans is encoded by the HP gene. [5][6] In blood plasma, haptoglobin binds with high affinity to free hemoglobin [7] released from erythrocytes, and thereby inhibits its deleterious oxidative activity. Compared to Hp, hemopexin binds to free heme. [8]

  3. Hemolytic anemia - Wikipedia

    en.wikipedia.org/wiki/Hemolytic_anemia

    Symptoms of hemolytic anemia are similar to the general signs of anemia.[2] General signs and symptoms include fatigue, pallor, shortness of breath, and tachycardia.[2] In small children, failure to thrivemay occur in any form of anemia. [6][7]In addition, symptoms related to hemolysis may be present such as chills, jaundice, dark urine, and an ...

  4. Hemolytic jaundice - Wikipedia

    en.wikipedia.org/wiki/Hemolytic_jaundice

    Type of jaundice. Hemolytic jaundice, also known as prehepatic jaundice, is a type of jaundicearising from hemolysisor excessive destruction of red blood cells, when the byproduct bilirubinis not excreted by the hepaticcells quickly enough.[1] Unless the patient is concurrently affected by hepatic dysfunctions or is experiencing hepatocellular ...

  5. Hemolytic–uremic syndrome - Wikipedia

    en.wikipedia.org/wiki/Hemolytic–uremic_syndrome

    [7] [18] [28] Early signs of systemic complement-mediated TMA include thrombocytopenia (platelet count below 150,000 or a decrease from baseline of at least 25%) [16] and evidence of microangiopathic hemolysis, which is characterized by elevated LDH levels, decreased haptoglobin, decreased hemoglobin, and/or the presence of schistocytes.

  6. Hemoglobinemia - Wikipedia

    en.wikipedia.org/wiki/Hemoglobinemia

    Hemoglobinemia (or haemoglobinaemia) is a medical condition in which there is an excess of hemoglobin in the blood plasma. This is an effect of intravascular hemolysis, in which hemoglobin separates from red blood cells, a form of anemia. Hemoglobinemia can be caused by intrinsic or extrinsic factors. When hemoglobinemia is internally caused ...

  7. Hemopexin family - Wikipedia

    en.wikipedia.org/wiki/Hemopexin_family

    The hemopexin family is a family of evolutionarily related proteins. Hemopexin-like repeats occur in vitronectin and some matrix metalloproteinases family (matrixins). [1] The HX repeats of some matrixins bind tissue inhibitor of metallopeptidases ( TIMPs ). Hemopexin ( EC 3.2.1.35) is a serum glycoprotein that binds haem and transports it to ...

  8. Serum protein electrophoresis - Wikipedia

    en.wikipedia.org/wiki/Serum_protein_electrophoresis

    Schematic representation of a protein electrophoresis gel. Serum protein electrophoresis (SPEP or SPE) is a laboratory test that examines specific proteins in the blood called globulins. [1] The most common indications for a serum protein electrophoresis test are to diagnose or monitor multiple myeloma, a monoclonal gammopathy of uncertain ...

  9. Gilbert's syndrome - Wikipedia

    en.wikipedia.org/wiki/Gilbert's_syndrome

    None typically needed [ 1 ] Frequency. ~5% [ 3 ] Gilbert syndrome (GS) is a syndrome in which the liver of affected individuals processes bilirubin more slowly than the majority. [ 1 ] Many people never have symptoms. [ 1 ] Occasionally jaundice (a slight yellowish color of the skin or whites of the eyes) may occur.