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Department

About the department

Department name (English):  Hematology Department

Department name (original): UOC Ematologia

Subnetworks of expertise:

  • Bleeding - Coagulation disorders

Healthcare provider: San Bortolo Hospital - Vicenza

Diseases covered by the department:

  • Essential thrombocythemia
  • Gaisböck syndrome
  • Rare coagulation disorder
  • Rare thrombotic disease of hematologic origin
  • Rare thrombotic disorder due to a coagulation factors defect
  • Rare thrombotic disorder due to a constitutional coagulation factors defect
  • Congenital factor XII deficiency
  • Familial thrombomodulin anomalies
  • Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
  • Rare hereditary thrombophilia
  • Rare thrombotic disorder due to an acquired coagulation factors defect
  • Catastrophic antiphospholipid syndrome
  • Heparin-induced thrombocytopenia
  • Protein S acquired deficiency
  • Acquired purpura fulminans
  • Simple cryoglobulinemia
  • Rare thrombotic disorder due to a platelet anomaly
  • Thrombotic thrombocytopenic purpura
  • Congenital thrombotic thrombocytopenic purpura
  • Acquired thrombotic thrombocytopenic purpura
  • Rare thrombotic disorder due to a constitutional platelet anomaly
  • Familial thrombocytosis
  • Hereditary thrombocytosis with transverse limb defect
  • Rare thrombotic disorder due to an acquired platelet anomaly
  • Rare hemorrhagic disorder
  • Rare hemorrhagic disorder due to a coagulation factors defect
  • Rare hemorrhagic disorder due to a constitutional coagulation factors defect
  • Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome
  • Hemophilia
  • Congenital factor V deficiency
  • Congenital fibrinogen deficiency
  • Congenital alpha2-antiplasmin deficiency
  • Congenital factor XIII deficiency
  • Von Willebrand disease
  • Congenital factor XI deficiency
  • Congenital plasminogen activator inhibitor type 1 deficiency
  • Congenital high-molecular-weight kininogen deficiency
  • Congenital prekallikrein deficiency
  • Combined deficiency of factor V and factor VIII
  • Congenital vitamin K-dependent coagulation factors deficiency
  • Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
  • East Texas bleeding disorder
  • Thrombomodulin-related bleeding disorder
  • Rare hemorrhagic disorder due to an acquired coagulation factor defect
  • Acquired prothrombin deficiency
  • Acquired hemophilia
  • Acquired von Willebrand syndrome
  • Rare hemorrhagic disorder due to a platelet anomaly
  • Rare hemorrhagic disorder due to a constitutional platelet anomaly
  • Rare hemorrhagic disorder due to a constitutional thrombocytopenia
  • Rare hemorrhagic disorder due to a qualitative platelet defect
  • Rare hemorrhagic disorder due to an acquired platelet anomaly
  • Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome
  • TAFRO syndrome
  • HELLP syndrome
  • Fetal and neonatal alloimmune thrombocytopenia
  • Autoimmune thrombocytopenia
  • Kasabach-Merritt syndrome

Health professionals

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