About the department
Department name (English): Hematology
Department name (original): Hematologie
Subnetworks of expertise:
- Myeloid malignancies
- Bleeding - Coagulation disorders
- Hemochromatosis and other iron disorders
- Bone marrow failure
Healthcare provider: Radboud University Medical Center Nijmegen
Diseases covered by the department:
- Tumor of hematopoietic and lymphoid tissues
- Mastocytosis
- Systemic mastocytosis
- Myeloid hemopathy
- Acute myeloid leukemia
- Myelodysplastic syndrome
- Myeloproliferative neoplasm
- Polycythemia vera
- Myelodysplastic/myeloproliferative disease
- Myeloid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB or FGFR1
- Polycythemia
- Primary familial polycythemia
- Secondary polycythemia
- Congenital secondary polycythemia
- Acquired secondary polycythemia
- Rare coagulation disorder
- Rare thrombotic disease of hematologic origin
- 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
- Congenital fibrinogen deficiency
- Familial afibrinogenemia
- Familial dysfibrinogenemia
- Familial hypofibrinogenemia
- Familial hypodysfibrinogenemia
- Congenital alpha2-antiplasmin deficiency
- Congenital factor XIII 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
- Congenital plasminogen activator inhibitor type 1 deficiency
- Combined deficiency of factor V and factor VIII
- 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 qualitative platelet defect
- Glanzmann thrombasthenia
- Scott syndrome
- P2Y12 defect
- Pseudo-von Willebrand disease
- Rare hemorrhagic disorder due to an acquired platelet anomaly
- Autoimmune thrombocytopenia
- Immune thrombocytopenic purpura
- Rare anemia
- Sideroblastic anemia
- Constitutional sideroblastic anemia
- X-linked sideroblastic anemia
- Autosomal recessive sideroblastic anemia
- Rare hemolytic anemia
- Rare constitutional hemolytic anemia
- Rare acquired hemolytic anemia
- Aplastic anemia
- Rare constitutional aplastic anemia
- Rare acquired aplastic anemia
- Rare deficiency anemia
- Rare acquired deficiency anemia
- Constitutional dyserythropoietic anemia
- Congenital dyserythropoietic anemia
- Rare iron overload
Service offered
- Prevention and genetic counseling
- Diagnostics
- Treatment and care
Patients covered