![]() Genes are the genetic material which code for all the proteins in the body, including the fibrinogen clotting factor. Some of this difference may relate to the various gene mutations that can be seen with this condition. Given the rarity of this disorder, we are still trying to understand out why some patients behave differently to others. This disorder causes different problems in different patients, for example, one person may experience blood clots while another may have problems with bleeding, while someone else again may have no noticeable problems at all. These disorders are inherited which means these patients are born with the problem. The AHCDO Executive Committee are pleased to announce that the successful application for 2022 isĭr Radha Ramanan for the project titled ‘Phenotypic characterisation and molecular profiling of congenital fibrinogen disorders: the Australian experience’.Ĭongenital fibrinogen disorders are rare disorders affecting of one of the major clotting proteins of the blood, fibrinogen. ![]() How to access deidentified data from the ABDR for research purposes. ![]() What is the Australian Bleeding Disorders Registry.National and International Collaborations.
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