scholarly journals A Unique Case of Popliteal Artery Thrombosis in Isolated Prothrombin Gene Mutation

Cureus ◽  
2020 ◽  
Author(s):  
Sakthivelavan Duraipandian-Sendiladibban ◽  
Kathleen Hoban ◽  
Sumathilatha Sakthi-Velavan ◽  
Ramesh Adhikari
Keyword(s):  
Gene Mutation ◽  
Popliteal Artery ◽  
Unique Case ◽  
Artery Thrombosis ◽  
Prothrombin Gene Mutation ◽  
Prothrombin Gene

Markers of activated coagulation in patients with factor V Leiden and/or G20210A prothrombin gene mutation

2002 ◽  
Vol 107 (1-2) ◽  
pp. 7-11 ◽  
Author(s):  
I Gouin-Thibault ◽  
R Arkam ◽  
S Nassiri ◽  
A de la Tourette ◽  
J Conard ◽  
...  
Keyword(s):  
Gene Mutation ◽  
Factor V Leiden ◽  
Factor V ◽  
Prothrombin Gene Mutation ◽  
Prothrombin Gene

scholarly journals Painless Livedoid Vasculopathy in a Patient with G20210A Prothrombin Gene Mutation

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
Aibek E. Mirrakhimov ◽  
Erwin Velasquez Kho ◽  
Alaa Ali
Keyword(s):  
Physical Examination ◽  
Gene Mutation ◽  
Case Reports ◽  
Arterial Disease ◽  
Skin Lesions ◽  
Livedoid Vasculopathy ◽  
Prothrombin Gene Mutation ◽  
Prothrombin Gene ◽  
Work Up ◽  
Caucasian Female

87 year old Caucasian female with chronic painless non-healing ulcers over malleoli was admitted to the hospital. On a physical examination, there were two bilateral and laterally located malleoli ulcers with no discharge. A thorough work up was done: lower extremities venous and arterial Doppler ultrasound did not show any evidence of venous and arterial disease respectively. Heterozygous G20210A Prothrombin gene mutation was found, and the patient was started on anticoagulation. This case reports highlights a possibility of a painless livedoid vasculopathy presentation in a patient without significant past thrombotic events. Therefore, it is important to consider livedoid vasculopathy in the differential in a patient with painless ulcerative, atrophic and/or nodular skin lesions over the shins and malleoli.

scholarly journals An investigation of the association of the prothrombin gene mutation and inflammatory bowel disease

2000 ◽  
Vol 118 (4) ◽  
pp. A1345
Author(s):  
Neil Haslam ◽  
Standen R. Graham ◽  
Jonathon L. Brown ◽  
Roland M. Valori ◽  
Christopher S. Probert
Keyword(s):  
Inflammatory Bowel Disease ◽  
Gene Mutation ◽  
Bowel Disease ◽  
Prothrombin Gene Mutation ◽  
Inflammatory Bowel ◽  
Prothrombin Gene
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