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. 2021 Sep;27(5):e641-e644.
doi: 10.1111/hae.14377. Epub 2021 Jul 13.

Afibrinogenemia with two compound heterozygous mutations in FGA gene

Guillaume Feugray  1 , Paul Billoir  1 , Alessandro Casini  2 , M Neerman-Arbez  3 , Virginie Barbay  1   4 , Pierre Chamouni  4 , Pascale Schneider  5 , Véronique Le Cam Duchez  1   4
Affiliations

Afibrinogenemia with two compound heterozygous mutations in FGA gene

Guillaume Feugray et al. Haemophilia. 2021 Sep.
No abstract available

Keywords: bleeding; cephalhaematoma; hereditary afibrinogenemia.

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References

REFERENCES

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    1. Palla R, Peyvandi F, Shapiro AD. Rare bleeding disorders: diagnosis and treatment. Blood. 2015;125(13):2052-2061.
    1. Casini A, von Mackensen S, Santoro C, et al. Clinical phenotype, fibrinogen supplementation and health-related quality of life in patients with afibrinogenemia. Blood. 2021.
    1. Joly B, Barbay V, Borg J-Y, Le Cam Duchez V. Comparison of markers of coagulation activation and thrombin generation test in uncomplicated pregnancies. Thromb Res. 2013;132(3):386-391.
    1. Adler G, Duchinski T, Jasinska A, Piotrowska U. Fibrinogen fractions in the third trimester of pregnancy and in puerperium. Thromb Res. 2000;97(6):405-410.

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