Year: 2008
Language: Farsi
The 2023 edition is available in: English, Spanish, French
This edition is also available in: Arabic, Russian, Simplified Chinese, Japanese
This edition of the resource has also been translated into the following language, with permission from the WFH, by NMOs: Polish, Bengali, Setswana
This patient handbook contains basic information about the inheritance, diagnosis, symptoms and management of von Willebrand disease.
This is not an official WFH translation. This resource has been translated with permission by a WFH National Member Organization (NMO), and is shared here with their kind permission. Translating organizations are encouraged to have translations reviewed by local experts, the WFH is not responsible for the translation or for any errors or changes to content from the original English edition. Patient organizations interested in translating a WFH resource must first obtain permission from the WFH, available here.
This patient handbook contains basic information about the inheritance, diagnosis, symptoms and management of fibrinogen disorders, including afibrinogenemia, hypofibrinogenemia, dysfibrinogenemia
Listen to this 90-minute webinar presented on September 21, 2023 to learn about von Willebrand disease (VWD) in low-resource settings.
Also Available In: Japanese This resource has also been translated into the following languages, with permission from the WFH, by
This edition is available in: English, Spanish, French The previous edition is also available in: Arabic, Russian, Simplified Chinese, Japanese
This patient handbook contains basic information about the inheritance, diagnosis, symptoms and management of inherited platelet function disorders, including Bernard-Soulier
The previous edition is also available in: Japanese The previous edition of this resource has also been translated into the
