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Clinical Features in 36 Patients Homozygous for the ARG 506 → GLN Factor V Mutation
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1997
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Homozygous Gln 506Vascular DiseaseGeneticsGenetic EpidemiologyPathologyClinical FeaturesMolecular GeneticsClinical GeneticsThrombosisVenous ThrombosisMendelian DisorderHematologyBleeding DisorderPublic HealthAtherosclerosisCardiologyVariant InterpretationMonogenic DisordersArg 506Arterial ThrombosisEpidemiologyThrombopoiesisAllelic VariantCardiovascular DiseaseGenetic DisorderMedical GeneticsCoagulopathyMedicine
We analyzed the clinical features of 36 patients homozygous for the Arg 506 to Gln factor V mutation and found a circumstantial event at risk for thrombosis in 29 of the 31 patients with thrombosis. The most frequent predisposing factors were the post-partum period and the use of oral contraceptives in women, and surgery in both sexes. Venous thrombosis recurred in 48% of the patients. One patient had a myocardial infarction at age 33 years, and also had an antiphospholipid syndrome. Homozygous Gln 506 mutation leads to far less severe thrombotic complications than homozygous protein C and protein S deficiencies and does not seem to predispose patients to arterial thrombosis.