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