Unexpected presentation of type 2N von Willebrand disease in pregnancy

Haemophilia

Volumn 6, Issue 6, 2000, Pages 696-697

  Dennis, M W ^a,b   Clough, V ^a,b   Toh, C H ^a,b  

^a ROYAL LIVERPOOL UNIVERSITY HOSPITAL   (United Kingdom)

^b Countess of Chester Hospital ^*  (United Kingdom)

Author keywords

Haemophilia A; Normandy variant; Pregnancy; Treatment; Von Willebrand disease

Indexed keywords

ARGININE; BLOOD CLOTTING FACTOR 8; DESMOPRESSIN; GLYCINE; OXYTOCIN; RECOMBINANT BLOOD CLOTTING FACTOR 8; RISTOCETIN; VON WILLEBRAND FACTOR;

ADULT; ARTICLE; CASE REPORT; CHILDBIRTH; CHROMOSOME INVERSION; DISEASE CLASSIFICATION; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC SCREENING; GESTATIONAL AGE; HEMOPHILIA A; HOMOZYGOSITY; HUMAN; INTRON; PARTIAL THROMBOPLASTIN TIME; POSTPARTUM HEMORRHAGE; PREGNANCY; PRIORITY JOURNAL; SOUTHERN BLOTTING; VON WILLEBRAND DISEASE; X CHROMOSOME INACTIVATION;

ADULT; DIAGNOSIS, DIFFERENTIAL; FEMALE; HEMOPHILIA A; HUMANS; PREGNANCY; PREGNANCY COMPLICATIONS, HEMATOLOGIC; VON WILLEBRAND DISEASE;

EID: 0033665168     PISSN: 13518216     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2516.2000.00428.x     Document Type: Article

References (7)

1. Pregnancy in women with Von Willebrand's disease or factor XI deficiency
2. Treatment of von Willebrand disease
3. Obstetric management in von Willebrand's disease; a report of 24 cases and a review of the literature
4. Guidelines on the therapeutic products to treat haemophilia and other hereditary Coagulation disorders
5. Biological effect of desmopressin in eight patients with type 2N ('Normandy') von Willebrand disease
6. Characterisation of type 2N von Willebrand disease using phenotypic and molecular techniques
7. Von Willebrand disease masquerading as haemophilia A