Departments

About the department

Department name (English): Haematology, Stem Cell Transplantation & Haemostasis

Department name (original): Hematologie, Stamceltransplantatie & Stolling

Subnetworks of expertise:

• Bleeding - Coagulation disorders

Healthcare provider: Universitair Ziekenhuis Antwerpen

Diseases covered by the department:

• 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
• Rare hereditary thrombophilia
• Hereditary thrombophilia due to congenital protein S deficiency
• Hereditary thrombophilia due to congenital protein C deficiency
• Hereditary thrombophilia due to congenital antithrombin deficiency
• Rare thrombotic disorder due to an acquired coagulation factors defect
• Catastrophic antiphospholipid syndrome
• Heparin-induced thrombocytopenia
• Protein S acquired deficiency
• Rare hemorrhagic disorder
• Rare hemorrhagic disorder due to a coagulation factors defect
• Rare hemorrhagic disorder due to a constitutional coagulation factors defect
• Hemophilia
• Hemophilia A
• Severe hemophilia A
• Moderately severe hemophilia A
• Mild hemophilia A
• Symptomatic form of hemophilia A in female carriers
• Hemophilia B
• Severe hemophilia B
• Moderately severe hemophilia B
• Mild hemophilia B
• Symptomatic form of hemophilia B in female carriers
• Congenital factor V deficiency
• Von Willebrand disease
• Von Willebrand disease type 1
• Von Willebrand disease type 2
• Von Willebrand disease type 2A
• Von Willebrand disease type 2B
• Von Willebrand disease type 2M
• Von Willebrand disease type 2N
• Von Willebrand disease type 3
• Congenital factor XI deficiency
• Combined deficiency of factor V and factor VIII
• Rare hemorrhagic disorder due to an acquired coagulation factor defect
• 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
• Isolated constitutional thrombocytopenia
• Isolated hereditary giant platelet disorder
• Severe autosomal recessive macrothrombocytopenia
• Bernard-Soulier syndrome
• Hereditary thrombocytopenia with normal platelets
• Congenital amegakaryocytic thrombocytopenia
• Isolated delta-storage pool disease
• Autosomal dominant thrombocytopenia with platelet secretion defect
• Rare hemorrhagic disorder due to a qualitative platelet defect
• Glanzmann thrombasthenia
• Ehlers-Danlos syndrome, fibronectinemic type
• P2Y12 defect
• Pseudo-von Willebrand disease
• Bleeding diathesis due to a collagen receptor defect
• Rare hemorrhagic disorder due to an acquired platelet anomaly
• Fetal and neonatal alloimmune thrombocytopenia
• Autoimmune thrombocytopenia
• Immune thrombocytopenic purpura
• Kasabach-Merritt syndrome

Service offered

• Prevention and genetic counseling
• Diagnostics

Patients covered

• Adults