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Table 3 Mutational state frequence for FV R506Q, PT G20210A, MTHFR C677T, PAI-1 4G/5G, ACE I/D genes in patients and healhty subjects (HS).

From: Benign intracranial hypertension associated to blood coagulation derangements

Gene coagulation mutations

Homozygous Wilde-type

Heterozygous

Homozygous Mutated

 

Patients (17)

HS (51)

Patients (17)

HS (51)

Patients (17)

HS (51)

FV R506Q

94%

98%

6%

2%

-

-

PT G20210A

94%

98%

6%

2%

-

-

MTHFR C677T

41%

57%

41%

31%

18%

12%

PAI-1 4G/5G

47%

30%

35%

51%

18%

19%

ACE I/D

30%

46%

47%

43%

23%

11%

  1. FV R506Q: factor V Leiden gene polimorphism
  2. PT G20210A: prothrombin G20210A gene polymorphism
  3. MTHFR C677T: Methylenetetrahydrofolate reductase C677T gene polymorphism
  4. PAI-1 4G/5G: plasminogen activator inihibitor 1 4G\5G gene polymorphism
  5. ACE I\D: angiotensin converting enzyme insertion\deletion gene polymorphism