SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Hämophiliezentrum am Universitätsklinikum des Saarlandes

Description of facility

Director / Spokesperson
Prof. Dr. med. H. Eichler, Prof. Dr. med. Furtwängler
Information
Care facility for adults and children
Description

Die Klinik für pädiatrische Onkologie und Hämatologie der Kliniken für Kinder- und Jugendmedizin betreut, zusammen mit dem Institut für Klinische Hämostaseologie und Transfusionsmedizin, Patienten aller Altersstufen mit Hämophilie A und B sowie mit weiteren schweren Gerinnungsstörungen. Die Fachkompetenz auf diesem Schwerpunkt hat sich speziell in den 1970er Jahren herausgebildet und laufend weiterentwickelt. So hat sich in den vergangenen Jahren ein überregional bedeutsames Hämophilie-Zentrum etabliert, das sich für die Maximalversorgung von Hämophilen in der Region Saar-Pfalz verantwortlich zeichnet und den Versorgungsgrad eines sog. Hemophilia Comprehensive Care Center entspricht. In Zusammenarbeit mit allen am Universitätsklinikum vertretenen medizinischen Fachdisziplinen ist eine optimale Hämophiliebetreuung mit Bezug auf Diagnostik und Therapie fest etabliert. Durch ein zentrales Team aus ärztlichen und pflegerischen Mitarbeitern mit umfassender Erfahrung und Fachkompetenz wird die Hämophilie-Betreuung auf der Basis modernster Standards praktiziert.

Consultation hours

Mo - Do 8:00 - 16:00 Uhr und Fr 8:00 - 14.00 Uhr nach Vereinbarung.

Care provisions

This facility offers the following
  • Genetic counselling
  • Diagnostic
  • Therapy

Contact

Prof. Dr. med. H. Eichler
06841 1622530
hermann.eichler@uks.eu
Website http://www.uniklinikum-saarland.de/de/einrichtungen/kliniken_institute/haemophilie_zentrum/

Secondary Contact

Prof. Dr. med. R. Furtwängler
06841 1628397
rhoikos.furtwaengler@uks.eu

Address

Ringstraße 52
66424 Homburg
Gebäude 1

Calculate route

Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Certificates 2

Preview of the assigned diseases 3

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

Provided care options 2

# Contact person
1
Pädiatrische Hämophilie MVZ-Ambulanz
Prof. Dr. Rhoikos Furtwängler

06841 1628409
Email
Website
Sprechzeiten: Mo - Fr 8:00 - 12:00 Uhr nach Vereinbarung.

2
Erwachsene Hämophilie MVZ-Ambulanz
Prof. Dr. med. H. Eichler

06841 1622532
Email
Website
Sprechzeiten: Mo - Do 8:00 - 16:00 Uhr, Fr 8:00 - 14:00 Uhr nach Vereinbarung.

7.34279567309358949.3121252Hämophiliezentrum am Universitätsklinikum des Saarlandes
Last updated: 01.12.2022