{"id":566,"date":"2024-01-14T21:05:26","date_gmt":"2024-01-14T20:05:26","guid":{"rendered":"https:\/\/www.francecoag.org\/presentation-of-france-coag\/project-francecoag\/target-population\/"},"modified":"2024-01-28T19:19:34","modified_gmt":"2024-01-28T18:19:34","slug":"target-population","status":"publish","type":"page","link":"https:\/\/www.francecoag.org\/en\/project-francecoag\/target-population\/","title":{"rendered":"Target population"},"content":{"rendered":"

The diseases eligible for the FranceCoag scheme are haemophilia, severe forms of rare HCM caused by another inherited coagulation protein deficiency (HCPD: afibrinogenemia, FII, FV, FVII, FX, FXI and FXIII deficiencies, FV+VIII, combined vitamin K-dependent factor deficiencies), symptomatic forms of Willebrand’s disease (WM) and inherited platelet diseases.<\/p>\n

The rate of monitoring and the size of the populations monitored are described in the table below. The FC acts as a registry for the most severe pathologies, i.e. :<\/p>\n

    \n
  1. FVIII and FIX deficiencies with levels \u2264 5% (severe or moderate haemophilia A and B, including Leyden B forms with FIX \u2264 5%);<\/li>\n
  2. the most severe forms of WM with a Willebrand Factor activity level (vWF:Act) \u2264 15% or an FVIII level \u2264 5% ;<\/li>\n
  3. congenital afibrinogenemia with a fibrinogen level < of 0.2 g\/l ;<\/li>\n
  4. FXIII deficiency with an < rate of 10% ;<\/li>\n
  5. Glanzmann thrombasthenia (TG);<\/li>\n
  6. Jean Bernard Soulier syndromes (SBS) ;<\/li>\n
  7. other registrable platelet diseases.<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"

    The diseases eligible for the FranceCoag scheme are haemophilia, severe forms of rare HCM caused by another inherited coagulation protein […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":565,"menu_order":6,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-566","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"\nTarget population - FranceCoag<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.francecoag.org\/en\/project-francecoag\/target-population\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Target population - FranceCoag\" \/>\n<meta property=\"og:description\" content=\"The diseases eligible for the FranceCoag scheme are haemophilia, severe forms of rare HCM caused by another inherited coagulation protein […]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.francecoag.org\/en\/project-francecoag\/target-population\/\" \/>\n<meta property=\"og:site_name\" content=\"FranceCoag\" \/>\n<meta property=\"article:modified_time\" content=\"2024-01-28T18:19:34+00:00\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.francecoag.org\\\/en\\\/project-francecoag\\\/target-population\\\/\",\"url\":\"https:\\\/\\\/www.francecoag.org\\\/en\\\/project-francecoag\\\/target-population\\\/\",\"name\":\"Target population - 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