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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. Intravascular hemolysis - Wikipedia

    en.wikipedia.org/wiki/Intravascular_hemolysis

    Nevertheless, if the binding capacities of haptoglobin and hemopexin are saturated [note 1], the remaining "free hemoglobin" in the plasma will be oxidized to met-hemoglobin eventually, and then further disassociates into free heme and others. [3] At this stage, the "free heme" will bind to albumin, forming met-hemalbumin.

  7. 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 ...

  8. Acute-phase protein - Wikipedia

    en.wikipedia.org/wiki/Acute-phase_protein

    Positive acute-phase proteins serve (as part of the innate immune system) different physiological functions within the immune system.Some act to destroy or inhibit growth of microbes, e.g., C-reactive protein, mannose-binding protein, [3] complement factors, ferritin, ceruloplasmin, serum amyloid A and haptoglobin.

  9. Proteins produced and secreted by the liver - Wikipedia

    en.wikipedia.org/wiki/Proteins_produced_and...

    All plasma proteins except Gamma-globulins are synthesised in the liver. [ 1 ] Human serum albumin, osmolyte and carrier protein. α-fetoprotein, the fetal counterpart of serum albumin. Soluble plasma fibronectin, forming a blood clot that stops bleeding. C-reactive protein, opsonin on microbes, [ 2 ] acute phase protein. Various other globulins.