Congenital afibrinogenemia

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Congenital afibrinogenemia
Congenital Afibrinogenemia presenting as antenatal intracranial bleed-T2 weighted coronal section with a mass effect on the right side with mid-line shift to the left side because of sub-dural bleeding

Congenital afibrinogenemia is a rare, genetically inherited blood fibrinogen disorder in which the blood does not clot normally due to the lack of fibrinogen, a blood protein necessary for coagulation.[1] This disorder is autosomal recessive, meaning that two unaffected parents can have a child with the disorder.[2] The lack of fibrinogen expresses itself with excessive and, at times, uncontrollable bleeding.[3]

Signs and symptoms

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]

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.[citation needed]


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.[citation needed]


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.[citation needed]


Diagnostic tests

When a problem of fibrinogen is suspected, the following tests can be ordered:

Blood fibrinogen levels of less than 0.1 g/L and prolonged bleeding test times are indicators of an individual having afibrinogenemia.[2]

A suspicion of congenital afibrinogenemia may appear on a platelet aggregation function test.

Platelet aggregation function by disorders and agonists   edit
ADP Epinephrine Collagen Ristocetin
P2Y receptor defect[9] (including Clopidogrel) Decreased Normal Normal Normal
Adrenergic receptor defect[9] Normal Decreased Normal Normal
Collagen receptor defect[9] Normal Normal Decreased or absent Normal
Normal Normal Normal Decreased or absent
Decreased Decreased Decreased Normal or decreased
Storage pool deficiency[10] Absent second wave Partial
Aspirin or aspirin-like disorder Absent second wave Absent Normal


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 theory, 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]

See also


  1. Neerman-Arbez, Marguerite; De Moerloose, Philippe (2007). "Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: An update and report of 10 novel mutations". Human Mutation. 28 (6): 540–53. doi:10.1002/humu.20483. PMID 17295221.
  2. 2.0 2.1 2.2 2.3 2.4 "Inherited Abnormalities of Fibrinogen: Background, Pathophysiology, Epidemiology". 2019-10-20. Archived from the original on 2021-10-31. Retrieved 2022-04-25. {{cite journal}}: Cite journal requires |journal= (help)
  3. 3.0 3.1 3.2 Vu, Dung; Bolton-Maggs, Paula H. B.; Parr, Jeremy R.; Morris, Michael A.; Moerloose, Philippe de; Neerman-Arbez, Marguerite (2003-12-15). "Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion". Blood. 102 (13): 4413–4415. doi:10.1182/blood-2003-06-2141. ISSN 0006-4971. PMID 12893758.
  4. 4.0 4.1 4.2 "Congenital Afibrinogenemia". DoveMed. Archived from the original on 2015-11-19. Retrieved 2015-11-12.
  5. 5.0 5.1 5.2 "Afibrinogenemia | Disease | Your Questions Answered | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". Archived from the original on 2015-12-22. Retrieved 2015-11-12.
  6. Neerman-Arbez, Marguerite; Vu, Dung; Abu-Libdeh, Bassam; Bouchardy, Isabelle; Morris, Michael A. (2003-05-01). "Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family". Blood. 101 (9): 3492–3494. doi:10.1182/blood-2002-10-3116. ISSN 0006-4971. PMID 12511408.
  7. McDowall, Jennifer (November 2006). "Fibrinogen". InterPro : Classification of protein families. Archived from the original on 19 June 2022. Retrieved 7 July 2020.
  8. Dysfibrinogenemia at eMedicine
  9. 9.0 9.1 9.2 9.3 9.4 Borhany, Munira; Pahore, Zaen; ul Qadr, Zeeshan; Rehan, Muhammad; Naz, Arshi; Khan, Asif; Ansari, Saqib; Farzana, Tasneem; Nadeem, Muhammad; Raza, Syed Amir; Shamsi, Tahir (2010). "Bleeding disorders in the tribe: result of consanguineous in breeding". Orphanet Journal of Rare Diseases. 5 (1). doi:10.1186/1750-1172-5-23. ISSN 1750-1172. PMID 20822539.
  10. 10.0 10.1 "Why Perform Platelet Aggregation?". Helena Biosciences. 2015
  11. "Congenital afibrinogenemia". Archived from the original on 2022-06-19. Retrieved 2015-11-12.
  12. Tziomalos K, Vakalopoulou S, Perifanis V, Garipidou V. Treatment of congenital fibrinogen deficiency: overview and recent findings. Vasc Health Risk Manag. 2009;5:843-848. doi:10.2147/vhrm.s5305
  13. Tziomalos K, Vakalopoulou S, Perifanis V, Garipidou V. Treatment of congenital fibrinogen deficiency: overview and recent findings. Vasc Health Risk Manag. 2009;5:843-848. doi:10.2147/vhrm.s5305
  14. "Factor I deficiency (Fibrinogen deficiency) - Canadian Hemophilia Society". Archived from the original on 2015-11-19. Retrieved 2015-11-12.
  15. "Congenital afibrinogenemia". Genetics Home Reference. 2015-11-09. Archived from the original on 2015-12-22. Retrieved 2015-11-12.
  16. "Search of: afibrinogenemia - List Results -". Archived from the original on 2015-12-22. Retrieved 2015-12-10.
  17. Gallastegui, N.; Kimble, E. L.; Harrington, T. J. (2015-09-01). "Resolution of fibrinogen deficiency in a patient with congenital afibrinogenemia after liver transplantation". Haemophilia. 22 (1): e48–e51. doi:10.1111/hae.12802. ISSN 1365-2516. PMID 26421965.

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