Year: 2024
Language: English
This patient handbook contains basic information about the inheritance, diagnosis, symptoms and management of fibrinogen disorders, including afibrinogenemia, hypofibrinogenemia, dysfibrinogenemia and hypodysfibrinogenemia.
This publication was created in collaboration with the International Fibrinogen Physician and Patients Association.
The WFH does not engage in the practice of medicine and under no circumstances recommends particular treatment for specific individuals. For diagnosis or consultation on a specific medical problem, the WFH recommends that you contact your physician or local treatment centre. Before administering any products, the WFH urges patients to check dosages with a physician or hemophilia centre staff, and to consult the pharmaceutical company’s printed instructions.
The WFH does not promote any particular pharmaceutical product and any mention of any commercial brand in this presentation is strictly for educational purposes.
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
The previous edition is also available in: Japanese The previous edition of this resource has also been translated into the
The previous edition is also available in: Japanese The previous edition of this resource has also been translated into the
