Familiar protein C deficiency and cerebral vein thrombosis in a young adult patient

1999 ◽  
Vol 20 (5) ◽  
pp. 333-334
Author(s):  
F. Villani ◽  
L. Chiapparini ◽  
D. Croci
2018 ◽  
Vol 58 (12) ◽  
pp. 764-766
Author(s):  
Yumeho Sugahara ◽  
Natsuki Ono ◽  
Eriko Morishita ◽  
Hiroshi Takashima

2011 ◽  
Vol 10 (2) ◽  
pp. 107-107

Acute Medicine 30 2011; 10(1): 29-31 V K Patel, B Warner, A Ceccherini & B Mearns An unusual cause of bilateral deep vein thrombosis in a young adult patient


2007 ◽  
Vol 14 (4) ◽  
pp. 415-420 ◽  
Author(s):  
Julide Altinisik ◽  
Omer Ates ◽  
Turgut Ulutin ◽  
Mujgan Cengiz ◽  
Nur Buyru

Several inherited polymorphisms are associated with risk of venous thrombosis, including mutation at codon 506 of the factor V gene, mutation at position 20210 of the prothrombin gene, and mutations in the protein C gene. In this study, genotyping for factor V, prothrombin, and protein C mutations was performed in 50 patients and 25 control subjects by polymerase chain reaction—based analysis. The prevalence of factor V and prothrombin mutations was not significantly different from that in the general population. Nine of the patients had heterozygous protein C mutation. There was a high prevalence of the mutated protein C allele in the pulmonary emboli group (42.8%). Protein C mutation incidence was higher in the pulmonary emboli group than in the deep vein thrombosis (8.33%) and cerebral vein thrombosis (16.1%) groups. These results indicate that patients with protein C deficiency have a greater risk of thrombosis than patients with factor V or prothrombin G20210A mutation.


1996 ◽  
Vol 76 (03) ◽  
pp. 477-478 ◽  
Author(s):  
I Martinelli ◽  
F R Rosendaal ◽  
J P Vandenbroucke ◽  
P M Mannucci

TH Open ◽  
2021 ◽  
Vol 05 (02) ◽  
pp. e171-e173
Author(s):  
Kiyoko Kanosue ◽  
Satomi Nagaya ◽  
Eriko Morishita ◽  
Masayoshi Yamanishi ◽  
Shinsaku Imashuku

AbstractA 78-year-old Japanese male with Clostridium perfringens septicemia and cholecystitis was found to have thrombosis in the left branch of intrahepatic portal vein as well as superior mesenteric vein. Visceral vein thrombosis (VVT) in this case was associated with protein C deficiency, due to a heterozygous mutation, p. Arg185Met. Our experience emphasizes that VVT, or other thromboembolic events, may occur in later life, triggered by environmental thrombosis risk factors, together with underlying hereditary protein C gene mutation.


2001 ◽  
Vol 90 (6) ◽  
pp. 1070-1072
Author(s):  
Emi Tajima ◽  
Hidetsugu Mihara ◽  
Motohiro Wakabayashi ◽  
Masaya Watarai ◽  
Kazutaka Sugamura ◽  
...  

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