Budd-Chiari syndrome in a paroxysmal nocturnal hemoglobinuria patient with coexistence of factor II and MTHFR mutations

J Thromb Haemost. 2005 May;3(5):1111. doi: 10.1111/j.1538-7836.2005.01283.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Ascites
  • Budd-Chiari Syndrome / diagnosis*
  • Factor V / genetics
  • Hemoglobinuria / complications*
  • Hemoglobinuria / diagnosis
  • Hemoglobinuria, Paroxysmal / complications*
  • Hemoglobinuria, Paroxysmal / diagnosis
  • Heterozygote
  • Humans
  • International Normalized Ratio
  • Male
  • Methylenetetrahydrofolate Dehydrogenase (NAD+) / genetics*
  • Mutation*
  • Prothrombin / genetics
  • Spleen / diagnostic imaging
  • Thrombophilia
  • Time Factors
  • Tomography, X-Ray Computed
  • Warfarin / pharmacology

Substances

  • Warfarin
  • Factor V
  • Prothrombin
  • Methylenetetrahydrofolate Dehydrogenase (NAD+)