Literature DB >> 21704322

Functional polymorphism in gamma-glutamylcarboxylase is a risk factor for severe neonatal hemorrhage.

Olivier M Vanakker1, Kris De Coen, Laura Costrop, Paul J Coucke, Piet Vanhaesebrouck, Anne De Paepe.   

Abstract

A neonate who received vitamin K (VK) supplementation then developed severe late-onset bleeding with abnormal prothrombin time and activated partial thromboplastine time. The bleeding was corrected after intravenous VK. Molecular analysis of the gamma-glutamylcarboxylase gene revealed a heterozygous single nucleotide polymorphism, which decreases carboxylase activity and induces VK-dependent coagulation deficiency.
Copyright © 2011 Mosby, Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21704322     DOI: 10.1016/j.jpeds.2011.04.044

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  1 in total

1.  Association of GGCX gene polymorphism with warfarin dose in atrial fibrillation population in Xinjiang.

Authors:  Xiayizha Kamali; Muhuyati Wulasihan; Yu-Chun Yang; Wu-Hong Lu; Zhi-Qiang Liu; Peng-Yi He
Journal:  Lipids Health Dis       Date:  2013-10-23       Impact factor: 3.876

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.