Klinik und Poliklinik für Kinder- und Jugendmedizin am Städtischen Klinikum Braunschweig Assigned diseases:
In the following you will find the diseases that are treated in this facility:
Acquired hemophilia
Acquired prothrombin deficiency
Acquired purpura fulminans
Acquired von Willebrand syndrome
Alpha delta granule deficiency
Alpha granule disease
Autoimmune thrombocytopenia
Autosomal dominant macrothrombocytopenia
Autosomal thrombocytopenia with normal platelets
Bernard-Soulier syndrome
Bleeding diathesis due to a collagen receptor defect
Bleeding diathesis due to glycoprotein VI deficiency
Bleeding diathesis due to integrin alpha2-beta1 deficiency
Bleeding diathesis due to thromboxane synthesis deficiency
Bleeding disorder due to P2Y12 defect
Bleeding disorder in hemophilia A carriers
Bleeding disorder in hemophilia B carriers
Combined deficiency of factor V and factor VIII
Congenital alpha2-antiplasmin deficiency
Congenital amegakaryocytic thrombocytopenia
Congenital factor II deficiency
Congenital factor V deficiency
Congenital factor VII deficiency
Congenital factor X deficiency
Congenital factor XI deficiency
Congenital factor XII deficiency
Congenital factor XIII deficiency
Congenital fibrinogen deficiency
Congenital high-molecular-weight kininogen deficiency
Congenital plasminogen activator inhibitor type 1 deficiency
Congenital prekallikrein deficiency
Congenital thrombotic thrombocytopenic purpura
Congenital vitamin K-dependent coagulation factors deficiency
Dense granule disease
East Texas bleeding disorder
Epstein syndrome
Essential thrombocythemia
Evans syndrome
Familial afibrinogenemia
Familial dysfibrinogenemia
Familial hypodysfibrinogenemia
Familial hypofibrinogenemia
Familial thrombocytosis
Familial thrombomodulin anomalies
Fechtner syndrome
Fetal and neonatal alloimmune thrombocytopenia
Gaisböck syndrome
Glanzmann thrombasthenia
Hemophilia
Hemophilia A
Hemophilia B
Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
Heparin-induced thrombocytopenia
Hereditary combined deficiency of vitamin K-dependent clotting factors
Hereditary thrombocytopenia with normal platelets
Hereditary thrombophilia due to congenital antithrombin deficiency
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
Immune thrombocytopenia
Immune-mediated thrombotic thrombocytopenic purpura
Isolated hereditary giant platelet disorder
MYH9-related disease
Macrothrombocytopenia with mitral valve insufficiency
May-Hegglin thrombocytopenia
Mediterranean macrothrombocytopenia
Mild hemophilia A
Mild hemophilia B
Moderate hemophilia A
Moderate hemophilia B
Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome
Paris-Trousseau thrombocytopenia
Protein S acquired deficiency
Pseudo-von Willebrand disease
Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome
Rare coagulation disorder
Rare hemorrhagic disorder
Rare hemorrhagic disorder due to a coagulation factors defect
Rare hemorrhagic disorder due to a constitutional coagulation factors defect
Rare hemorrhagic disorder due to a constitutional platelet anomaly
Rare hemorrhagic disorder due to a constitutional thrombocytopenia
Rare hemorrhagic disorder due to a platelet anomaly
Rare hemorrhagic disorder due to a qualitative platelet defect
Rare hemorrhagic disorder due to an acquired coagulation factor defect
Rare hemorrhagic disorder due to an acquired platelet anomaly
Rare hereditary thrombophilia
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 thrombotic disorder due to a constitutional platelet anomaly
Rare thrombotic disorder due to a platelet anomaly
Rare thrombotic disorder due to an acquired coagulation factors defect
Rare thrombotic disorder due to an acquired platelet anomaly
Scott syndrome
Sebastian syndrome
Severe hemophilia A
Severe hemophilia B
Severe hereditary thrombophilia due to congenital protein C deficiency
Severe hereditary thrombophilia due to congenital protein S deficiency
Simple cryoglobulinemia
Stormorken-Sjaastad-Langslet syndrome
Thrombocythemia with distal limb defects
Thrombocytopenia with congenital dyserythropoietic anemia
Thrombocytopenia-absent radius syndrome
Thrombotic thrombocytopenic purpura
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
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia
X-linked thrombocytopenia with normal platelets