Literature DB >> 10356151

Prothrombin G20210A mutation in a child with spinal cord infarction.

G Young1, K A Krohn, R J Packer.   

Abstract

Prothrombin G20210A is a newly described common mutation that is associated with an increased risk of arterial and venous thrombosis. We describe a healthy child heterozygous for this prothrombin mutation who had a spinal cord infarct with no other prothrombotic risk factors.

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Year:  1999        PMID: 10356151     DOI: 10.1016/s0022-3476(99)70298-2

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


  3 in total

Review 1.  Ischemic spinal cord infarction in children without vertebral fracture.

Authors:  Jessica R Nance; Meredith R Golomb
Journal:  Pediatr Neurol       Date:  2007-04       Impact factor: 3.372

2.  Spinal cord infarction in a young adult: What is the culprit?

Authors:  Maria Khoueiry; Hussein Moussa; Raja Sawaya
Journal:  J Spinal Cord Med       Date:  2019-10-09       Impact factor: 1.985

3.  American College of Medical Genetics consensus statement on factor V Leiden mutation testing.

Authors:  W W Grody; J H Griffin; A K Taylor; B R Korf; J A Heit
Journal:  Genet Med       Date:  2001 Mar-Apr       Impact factor: 8.822

  3 in total

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