Name: Jenny
Surname: Goudemand
Academic title: Pr
Which is your area of expertise for the "Disease/group of diseases"?
Specify your expertise for the "Disease/group of diseases" (eg SCT, Molecular diagnosis):
Expertise in the phenotypic and genotypic diagnosis of von Willebrand disease (VWD) Treatment of congenital or acquired VWD or severe clotting deficiencies Treatment of haemophilia
Diseases:
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 Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome 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 Congenital high-molecular-weight kininogen deficiency Congenital prekallikrein deficiency Combined deficiency of factor V and factor VIII Congenital vitamin K-dependent coagulation factors deficiency Congenital factor VII deficiency Congenital factor II deficiency Congenital factor X deficiency Hereditary combined deficiency of vitamin K-dependent clotting factors Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation East Texas bleeding disorder Thrombomodulin-related bleeding disorder Rare hemorrhagic disorder due to an acquired coagulation factor defect Acquired prothrombin deficiency Acquired hemophilia Acquired von Willebrand syndrome
Which is your patient age coverage?
Member Representative
Subnetwork representative:
Name english: CHU de Lille
Name original: CHU de Lille
Name english: CHU de Lille
Name original: CHU de Lille
English name | Original name | Subnetworks of expertise | Healthcare provider |
---|---|---|---|
Clinical Haemostasis and Transfusion | Service d’Hémostase Clinique et Transfusion | Bleeding - Coagulation disorders | CHU de Lille |