Congenital afibrinogenemia: Difference between revisions
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'''Congenital afibrinogenemia''' is a rare inherited blood disorder in which the [[blood]] does not clot normally due to a lack of or a malfunction involving [[fibrinogen]], a [[protein]] necessary for [[coagulation]]. | '''Congenital afibrinogenemia''' is a rare inherited blood disorder in which the [[blood]] does not clot normally due to a lack of or a malfunction involving [[fibrinogen]], a [[protein]] necessary for [[coagulation]]. | ||
====Drugs causing afibrinogenemia==== | |||
* [[Oxytocin]] | |||
==External links== | ==External links== | ||
Latest revision as of 20:11, 10 December 2014
Template:DiseaseDisorder infobox
Congenital afibrinogenemia is a rare inherited blood disorder in which the blood does not clot normally due to a lack of or a malfunction involving fibrinogen, a protein necessary for coagulation.
Drugs causing afibrinogenemia
External links