Literature DB >> 26407137

Umbilical bleeding: a presenting feature for congenital afibrinogenemia.

Hassan Abolghasemi1, Ehsan Shahverdi.   

Abstract

Congenital afibrinogenemia is a very rare inherited coagulation disorder characterized by absence of plasma fibrinogen (factor I). There are only about 250 cases reported in the world literature. We describe a case of congenital afibrinogenemia which presented as an umbilical cord bleeding.

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Year:  2015        PMID： 26407137     DOI： 10.1097/MBC.0000000000000368

Source DB:  PubMed          Journal:  Blood Coagul Fibrinolysis        ISSN： 0957-5235            Impact factor:   1.276


  3 in total

Review 1.  Clinical Consequences and Molecular Bases of Low Fibrinogen Levels.

Authors:  Marguerite Neerman-Arbez; Alessandro Casini
Journal:  Int J Mol Sci       Date:  2018-01-08       Impact factor: 5.923

2.  Combined occurrence of Bernard-Soulier syndrome and prekallikrein deficiency.

Authors:  Ehsan Shahverdi; Hassan Abolghasemi; Minoo Ahmadinejad
Journal:  Blood Res       Date:  2017-09-25

Review 3.  Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype.

Authors:  Tomas Simurda; Monika Brunclikova; Rosanna Asselta; Sonia Caccia; Jana Zolkova; Zuzana Kolkova; Dusan Loderer; Ingrid Skornova; Jan Hudecek; Zora Lasabova; Jan Stasko; Peter Kubisz
Journal:  Int J Mol Sci       Date:  2020-06-29       Impact factor: 5.923
  3 in total

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