Skip navigation

Refine by Type

Results 1 - 5 of 5 for Afibrinogenemia
  1. Genetics Home Reference: Congenital afibrinogenemia From the National Institutes of Health (National Library of Medicine)  
    ... Research studies OMIM Genetic disorder catalog Conditions > Congenital afibrinogenemia On this page: Description Genetic changes Inheritance Diagnosis ... Glossary definitions Reviewed September 2014 What is congenital afibrinogenemia? Congenital afibrinogenemia is a bleeding disorder caused by ...
  2. Congenital afibrinogenemia is a rare, inherited blood disorder in which the blood does not clot normally. It occurs when ... only one abnormal gene from their parents. Congenital afibrinogenemia can occur in males or females. The main ...
  3. Fibrinogen Test (American Association for Clinical Chemistry)  
    ... production due to an inherited condition such as afibrinogenemia or hypofibrinogenemia or to an acquired condition such ... performed for those with inherited dysfibrinogenemia, hypofibrinogenemia , or afibrinogenemia to identify the genetic mutation responsible. Testing for ...
  4. Thrombin Time (American Association for Clinical Chemistry)  
    ... time may indicate decreased fibrinogen level (hypofibrinogenemia or afibrinogenemia) and/or abnormal fibrinogen function (dysfibrinogenemia). Conditions such ...
  5. Bleeding Disorders (National Library of Medicine)  
    Normally, if you get hurt, your body forms a blood clot to stop the bleeding. For blood to clot, your body needs cells called platelets and proteins known as clotting ...