Congenital hypersensitivity to vitamin K antagonists due to FIX propeptide mutation at locus -10: A (not so) rare cause of bleeding under oral anticoagulant therapy in Switzerland

Swiss Medical Weekly

Volumn 138, Issue 7-8, 2008, Pages 100-107

  Ulrich, Silvia ^a,c   Brand, Brigitte ^a   Speich, Rudolf ^a   Oldenburg, Johannes ^b   Asmis, Lars ^a  

^a UNIVERSITY HOSPITAL ZURICH   (Switzerland)

^b UNIVERSITY HOSPITAL BONN   (Germany)

^c Department of Internal Medicine ^*  (Switzerland)

Author keywords

Bleeding; Coumarin sensitivity; Factor IX gene; Oral anticoagulation

Indexed keywords

ACETYLSALICYLIC ACID; ALANINE; ANTIVITAMIN K; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; BLOOD CLOTTING FACTOR 10; BLOOD CLOTTING FACTOR 7; BLOOD CLOTTING FACTOR 9; BLOOD CLOTTING FACTOR 9 CONCENTRATE; BLOOD CLOTTING FACTOR 9 PROPEPTIDE; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; LOOP DIURETIC AGENT; NONSTEROID ANTIINFLAMMATORY AGENT; PHENPROCOUMON; PROTEIN PRECURSOR; PROTHROMBIN; SPIRONOLACTONE; THREONINE; UNCLASSIFIED DRUG;

AGED; AMINO ACID SUBSTITUTION; ANTICOAGULANT THERAPY; ARTICLE; BLEEDING; BLEEDING TENDENCY; BLOOD CLOTTING DISORDER; BLOOD CLOTTING TEST; CLINICAL ARTICLE; CONTROLLED STUDY; CONVALESCENCE; DISEASE SEVERITY; DRUG DOSE REDUCTION; DRUG HYPERSENSITIVITY; DRUG WITHDRAWAL; FAMILY HISTORY; FAMILY STUDY; FEMALE; FOUNDER EFFECT; GENE LOCUS; GENE MUTATION; GERMANY; HUMAN; INTERNATIONAL NORMALIZED RATIO; MALE; MUTATIONAL ANALYSIS; PARTIAL THROMBOPLASTIN TIME; SWITZERLAND; THROMBOEMBOLISM; X CHROMOSOME RECESSIVE DISORDER; X CHROMOSOME RECESSIVE INHERITANCE;

EID: 40349101933     PISSN: 14247860     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (21)