Congenital afibrinogenemia

As this is a disorder that is present in an individual from birth, there are no warning signs to look for. The first symptom usually seen is hemorrhage from the umbilical cord that is difficult to stop.[2]

Other symptoms include:[4]

• Nasal and oral mucosa bleeds
• Gastrointestinal bleeding
• Excessive/spontaneous bleeding or bruising from minor injury
• Prolonged menstruation in women
• Spontaneous abortion during pregnancy
• CNS hemorrhaging[5]

Spontaneous bleeding of the mouth, nose, and gastrointestinal tract are common. Since blood clots can not be formed, minor injuries tend to lead to excessive bleeding or bruising. The biggest concern for individuals with afibrinogenemia is CNS hemorrhage, bleeding in the brain, which can be fatal. Many of these symptoms are chronic, and will continue to occur for the entirety of the affected individual's life.

A missense or nonsense mutation to the genes that code for the fibrinogen protein are affected. Usually the mutation leads to an early stop in the production of the protein.[3] Due to the problem being genetically based, there is no way to prevent the disease. Individuals can get genetic testing done to see if they are a carrier of the trait, and if so may choose to complete genetic counseling to better understand the disorder and help manage family planning. Parents can choose to do prenatal genetic testing for the disorder to determine if their child will have the disease.[6] The only risk factor is if both parents of a child carry the recessive allele linked to the disorder.

Individuals with the disorder have a mutation to their fibrinogen gene that prevents the formation of the protein.[3] In normal conditions, fibrinogen is converted to fibrin when it is cleaved by the enzyme thrombin in the blood. The newly formed fibrin forms a fiber-rich network that helps trap red blood cells to start the coagulation process and form a clot.[7] Since there is no fibrinogen present during afibrinogenemia, fibrin can not be formed to aid in this process.

The most common treatment is fibrinogen replacement therapy, including cryoprecipitate, blood plasma, and fibrinogen concentration transfusions to help with bleeding episodes or prior to surgery.[11] Although some thrombotic complications have been reported following replacement therapy, transfusions of fibrinogen concentrate are widely considered to be the most beneficial. Fibrinogen concentrate is pure, contains a known quantity of fibrinogen, is virally inactivated, and is transfused in small amounts. [12] There is a lower chance of allergic reaction in response to transfusion. Alternatively, cryoprecipitate contains other coagulation factors, factors VIII, XIII, and von Willebrand factor. [13] There are no known cures or forms of holistic care to date. Most complications arise from the symptoms of the disorder.[5]

As there is not much data out on the life expectancy of an individual with afibrinogenemia, it is difficult to determine the average lifespan. However, the leading cause of death thus far is linked to CNS hemorrhage and postoperative bleeding.[5]

It was first described in 1920 by German doctors, Fritz Rabe and Eugene Salomon, studying a bleeding disorder presenting itself in a child from birth.[14] This disorder may also be simply called afibrinogenemia or familial afibrinogenemia.[4] About 1 in 1 million individuals are diagnosed with the disease; typically at birth.[15] Both males and females seem to be affected equally,[2] but it has a higher occurrence in regions where consanguinity is prevalent.[4]

Currently research is based in pharmacological treatments.[16] A case from 2015 was seen in which congenital afibrinogenemia was resolved in a patient after receiving a liver transplant.[17]

• Factor I Deficiency