SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Klinik und Poliklinik für Kinder- und Jugendmedizin am Städtischen Klinikum Braunschweig

Description of facility

Director / Spokesperson
Prof. Dr. Hans Georg Koch
Information
Care facility for children
Description
Die Klinik für Kinder- und Jugendmedizin übernimmt mit ihren 90 Betten die stationäre Versorgung von Kindern und Jugendlichen in der Region Braunschweig. Es werden pro Jahr etwa 6000 Patienten stationär und ca. 10.000 Patienten ambulant behandelt. Die Klinik bietet das gesamte Spektrum einer Klinik der Maximalversorgung und behandelt alle Erkrankungen des Neugeborenen-, Kindes- und Jugendalters. Die Klinik befindet sich an zwei Standorten. Neben dem Hauptstandort in der Holwedestraße befindet sich die Kinder-Intensivstation in räumlicher Nähe zur Frauenklinik am Standort Celler Straße und bildet gemeinsam mit der Frauenklinik ein Perinatalzentrum zur Versorgung von Früh- und Neugeborenen (Level I). In diesem Perinatalzentrum können Frühgeborene aller Reifegrade, auch extrem kleine Frühgeborene mit Geburtsgewichten unter 500g jederzeit kompetent versorgt werden.

Care provisions

This facility offers the following
  • Diagnostic
  • Therapy

Contact

Sekretariat
0531 5954909
0531 5954914
kinderklinik@skbs.de
Website https://klinikum-braunschweig.de/klinikwegweiser.php?object=contact&id_object=494&tab=ueberblick

Address

Salzdahlumer Straße 90
38126 Braunschweig

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Certificates 2

Preview of the assigned diseases 1

Von Willebrand disease type 3 Rare thrombotic disease of hematologic origin Rare hemorrhagic disorder due to an acquired platelet anomaly X-linked dyserythropoietic anemia with abnormal platelets and neutropenia Familial hypofibrinogenemia Alpha granule disease Dense granule disease Severe hemophilia B Scott syndrome Sebastian syndrome Rare thrombotic disorder due to a coagulation factors defect Acquired von Willebrand syndrome Moderate hemophilia B Severe hemophilia A Hemophilia B Mild hemophilia B Hemophilia A Rare thrombotic disorder due to a constitutional coagulation factors defect Familial dysfibrinogenemia Rare thrombotic disorder due to a platelet anomaly Moderate hemophilia A Familial afibrinogenemia Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Rare thrombotic disorder due to an acquired coagulation factors defect Bleeding diathesis due to glycoprotein VI deficiency Rare hemorrhagic disorder due to a constitutional coagulation factors defect Immune thrombocytopenia Bernard-Soulier syndrome Mild hemophilia A Bleeding diathesis due to integrin alpha2-beta1 deficiency Rare hemorrhagic disorder due to a constitutional platelet anomaly Autoimmune thrombocytopenia Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Congenital thrombotic thrombocytopenic purpura East Texas bleeding disorder Immune-mediated thrombotic thrombocytopenic purpura Pseudo-von Willebrand disease Congenital vitamin K-dependent coagulation factors deficiency Gaisböck syndrome Acquired prothrombin deficiency Protein S acquired deficiency Familial thrombocytosis Simple cryoglobulinemia Bleeding diathesis due to a collagen receptor defect Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Acquired hemophilia Glanzmann thrombasthenia Rare thrombotic disorder due to a constitutional platelet anomaly May-Hegglin thrombocytopenia Paris-Trousseau thrombocytopenia X-linked thrombocytopenia with normal platelets Fetal and neonatal alloimmune thrombocytopenia Rare thrombotic disorder due to an acquired platelet anomaly Combined deficiency of factor V and factor VIII Bleeding diathesis due to thromboxane synthesis deficiency Hemophilia Macrothrombocytopenia with mitral valve insufficiency Familial hypodysfibrinogenemia Rare hereditary thrombophilia Essential thrombocythemia Hereditary thrombocytopenia with normal platelets Thrombotic thrombocytopenic purpura Isolated hereditary giant platelet disorder Congenital amegakaryocytic thrombocytopenia Thrombocytopenia-absent radius syndrome Autosomal thrombocytopenia with normal platelets Evans syndrome Familial thrombomodulin anomalies Heparin-induced thrombocytopenia Alpha delta granule deficiency Congenital factor II deficiency Congenital factor V deficiency Congenital factor VII deficiency Congenital factor X deficiency Congenital plasminogen activator inhibitor type 1 deficiency Acquired purpura fulminans Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Congenital factor XI deficiency Congenital factor XII deficiency Congenital factor XIII deficiency Severe hereditary thrombophilia due to congenital protein S deficiency Congenital fibrinogen deficiency Severe hereditary thrombophilia due to congenital protein C deficiency Epstein syndrome Autosomal dominant macrothrombocytopenia Stormorken-Sjaastad-Langslet syndrome Congenital prekallikrein deficiency Thrombocythemia with distal limb defects Bleeding disorder in hemophilia A carriers Rare hemorrhagic disorder Bleeding disorder in hemophilia B carriers Congenital high-molecular-weight kininogen deficiency Fechtner syndrome Thrombocytopenia with congenital dyserythropoietic anemia Bleeding disorder due to P2Y12 defect Congenital alpha2-antiplasmin deficiency Hereditary thrombophilia due to congenital antithrombin deficiency Rare hemorrhagic disorder due to a coagulation factors defect Von Willebrand disease Rare hemorrhagic disorder due to a qualitative platelet defect Rare hemorrhagic disorder due to a constitutional thrombocytopenia Rare coagulation disorder Von Willebrand disease type 2 Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Von Willebrand disease type 1 Mediterranean macrothrombocytopenia Von Willebrand disease type 2A Hereditary combined deficiency of vitamin K-dependent clotting factors Rare hemorrhagic disorder due to a platelet anomaly Von Willebrand disease type 2M Von Willebrand disease type 2B Rare hemorrhagic disorder due to an acquired coagulation factor defect Von Willebrand disease type 2N MYH9-related disease

Provided care options 1

# Contact person
1
Spezialsprechstunde für Gerinnungsstörungen
Dr. med. Wolfgang Eberl

0531 5954917
Email
Website
Sprechzeiten nach Vereinbarung.

10.54732837965055152.23775838903423Klinik und Poliklinik für Kinder- und Jugendmedizin am Städtischen Klinikum Braunschweig
Last updated: 22.06.2023