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185 Possible Causes for Haptoglobin Decreased, No Liver Disease

  • Liver Failure

    There are many causes of liver disease; the most common are infections with viruses and alcohol.[] […] of the liver Fatty liver disease Galactosemia Gallstones Gilbert's syndrome Hemochromatosis Liver cancer Liver disease in pregnancy Neonatal hepatitis Primary biliary cirrhosis[] Enlarged liver According to the Mayo Clinic , an enlarged liver (or hepatomegaly) isn't a disease itself, but a sign of an underlying serious problem, such as liver disease[]

  • Wilson Disease

    The liver in Wilson disease may demonstrate a wide range of damage patterns.[] (Hepatology 2016;63:1828-1841). 2015 by the American Association for the Study of Liver Diseases.[] KEYWORDS: Wilson disease; acute liver failure; end-stage liver disease; liver transplant[]

  • Chronic Active Hepatitis B

    liver disease.[] Abstract The case of a 52-year-old male with chronic active type B hepatitis in whom severe exacerbation of liver disease was associated with interferon alpha treatment is[] This suggests that the role of HCV is probably important as the cause of persistent liver disease. 4) The detection of HBV-DNA by dot-blot and HCV-RNA by PCR could help to[]

  • Massive Hepatic Necrosis

    Neonatal hemochromatosis (NH) is an uncommon disorder clinicopathologically defined by severe liver disease of intrauterine onset associated with extrahepatic siderosis that[] Hepatic necrosis after ethanol ablation for hepatocellular carcinoma (HCC), although rare, is well known and described, particularly in patients with chronic liver disease[] This article deals with medical liver disease. An introduction to the liver and approach is found in the liver article.[]

  • Glycogen Storage Disease Type 1

    Make optimal use of the newest techniques, technologies, and treatments with Sleisenger and Fordtran's Gastrointestinal and Liver Disease - the indispensable information source[] PMID: 1333075 A new variant of type IV glycogenosis: deficiency of branching enzyme activity without apparent progressive liver disease.[] Are there specific foods or diet which would help my liver disease? Is my diagnosis of GSD genetic and if so, should others in my family be tested?[]

  • Disseminated Intravascular Coagulation

    Thrombotic complications of DIC occur more often with chronic underlying diseases; the coexistence of liver disease enhances the severity of DIC.[] disease Pregnancy complications (such as placenta that is left behind after delivery) Recent surgery or anesthesia Severe tissue injury (as in burns and head injury) Large[] Tabs Content Clinical Overview Diagnosis Indications for Testing Severe disease including sepsis, obstetrical disease, malignancy, liver disease, AND bleeding or microthrombi[]

  • Thalassemia

    Reticulocytes, LDH and bilirubin are increased; haptoglobin is decreased.[] Patients with liver disease, renal disease, type 1 diabetes, malabsorption, hypercortisolism, malignancy, and contraindication for MRI were excluded.[] Heart and Liver Diseases Regular blood transfusions are a standard treatment for thalassemias. Transfusions can cause iron to build up in the blood (iron overload).[]

  • Congestive Heart Failure

    […] fibrous dysplasia, anemia, carcinoid syndrome, arteriovenous fistulas–trauma, Paget's disease of bone, hemangiomatosis, glomerulonephritis, hemodialysis, liver disease–alcohol-related[] , liver disease, and peripheral vascular disease (data posted at ).[] Remind your doctor or healthcare provider if you have a history of diabetes, liver, kidney, or heart disease.[]

  • Hereditary Spherocytosis

    Routine chemistry testing  Bilirubin: Increased  Indirect bilirubin  Urine urobilinogen: increased  Methaemalbumin: Increased  LDH: Increased  Haptoglobin: Decreased[] Gilbert syndrome (GS) is an autosomal dominant disorder characterized with intermittent hyperbilirubinemia without any other sign and symptom of liver disease as a result[] This is a potential cause of heart muscle damage and liver disease.[]

  • Autoimmune Hemolytic Anemia

    , and haptoglobin decreased to less than 8 mg/dL.[] disease, in patients with GCH-AHA.[] Haptoglobin: -Decreased with intravascular hemolysis. Urine analysis: -When hemolysis has been acute and brisk the patient may have hemoglobinuria.[]

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