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Congenital afibrinogenemia in a patient with vascular abnormalities and a novel variant: clinical-molecular description and literature review

  • Published:2020-01 Issue:1 Volume:31 Page:65-70
  • ISSN:0957-5235
  • Container-title:Blood Coagulation & Fibrinolysis
  • language:en
  • Short-container-title:

Author:

Virmond Luiza A.,Micheletti Cecilia,Pinto Christiane M.S.,Soares Maria F.F.,Milanezi Fernanda,Nakano Viviane,Perrone Eduardo

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology,General Medicine

Reference21 articles.

1. Congenital afibrinogenemia: from etiopathogenesis to challenging clinical management;Stanciakova;Expert Rev Hematol,2016

2. Congenital afibrinogenemia: report of three cases;Anwar;J Thromb Haemost,2005

3. Congenital afibrinogenemia; a rare disorder with unusual clinical manifestations;Shahverdi;J Blood Disord Symptoms Treat,2018

4. Identification and characterization of novel mutations implicated in congenital fibrinogen disorders;Smith;Res Pract Thromb Haemost,2018

5. Clinical consequences and molecular bases of low fibrinogen levels;Neerman-Arbez;Int J Mol Sci,2018

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