What is an Afibrinogenemia?

by andywalsh | April 19, 2019 11:26 pm

It is defined as a disorder in which there is an absence of the clotting of blood. It is rare and inherited in form. There is an absence or mal function of the fibrinogen which is a protein for the coagulation. It is also known as the congenital afibrinogenemia. Factor one is also known as the fibrinogen. It is autosomal recessive in nature and has the ability to express itself. There is a large amount of bleeding when the individual is born. It occurs from the umbilical cord and also leads to easy bruising and bleeding after the circumcision.

What are the signs and symptoms of Afibrinogenemia?

It includes the large amount of bleeding when the individual is born. It occurs from the umbilical cord and also leads to easy bruising and bleeding after the circumcision.

What is the diagnosis of Afibrinogenemia?

It includes the PT, PTT, reptilase time, thrombin time and the presence of fibrinogen level in blood.

What is the treatment of Afibrinogenemia?

No specific treatment for this disorder.

Source URL: https://alldiseases.org/afibrinogenemia/