A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene

A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene

Abstract Congenital prothrombin deficiency is an extremely rare, autosomal recessive bleeding disorder with a prevalence of 1 in 2 million individuals. Here, we report a case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene (F2), affecting the heavy B chain....

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Bibliographic Details
Main Authors: Eman M. Mansory, Pratibha Bhai, Alan Stuart, Lori Laudenbach, Bekim Sadikovic, Alejandro Lazo‐Langner
Format: Article
Language:English
Published: Wiley 2021-05-01
Series:Research and Practice in Thrombosis and Haemostasis
Subjects:
bleeding disorder
dysprothrombinemia
hypoprothrombinemia
prothrombin deficiency
prothrombin mutation
Online Access:https://doi.org/10.1002/rth2.12510

Internet

https://doi.org/10.1002/rth2.12510

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