Bleeding in carriers of hemophilia

Blood

Volumn 108, Issue 1, 2006, Pages 52-56

  Plug, Iris ^b   Mauser Bunschoten, Eveline P ^b   Bröcker Vriends, Annette H J T ^b   Van Amstel, Hans Kristian Ploos ^b   Van Der Bom, Johanna G ^b   Van Diemen Homan, Joanna E M ^b   Willemse, José ^b   Rosendaal, Frits R ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 9;

ADULT; AGED; ARTICLE; BLEEDING; COMPARATIVE STUDY; CONTROLLED STUDY; DEMOGRAPHY; FEMALE; HEMOPHILIA; HEMOPHILIA A; HEMOPHILIA B; HUMAN; INJURY; LOGISTIC REGRESSION ANALYSIS; MAJOR CLINICAL STUDY; MENSTRUAL CYCLE; NETHERLANDS; PRIORITY JOURNAL; QUESTIONNAIRE; RISK FACTOR; TONSILLECTOMY; TOOTH EXTRACTION;

EID: 33745632764     PISSN: 00064971     EISSN: 00064971     Source Type: Journal    
DOI: 10.1182/blood-2005-09-3879     Document Type: Article

References (16)

1. Rizza CR, Rhymes IL, Austen DE, Kernoff PB, Aroni SA. Detection of carriers of haemophilia: a 'blind' study. Br J Haematol. 1975;30:447-456.
2. Brocker-Vriends AH, Bakker E, Kanhai HH, et al. The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B. Ann Hematol. 1992;64:2-11.
3. Tedgard U. Carrier testing and prenatal diagnosis of haemophilia - utilisation and psychological consequences. Haemophilia. 1998;4:365-369.
4. Veltkamp JJ, Drion EF, Loeliger EA. Detection of the carrier state in hereditary coagulation disorders. I. Thromb Diath Haemorrh. 1968;19:279-303.
5. Lyon MF. Sex chromatin and gene action in the mammalian X chromosome. Am J Hum Genet. 1962;14:135-148.
6. Orstavik KH, Scheibel E, Ingerslev J, Schwartz M. Absence of correlation between X chromosome inactivation pattern and plasma concentration of factor VIII and factor IX in carriers of haemophilia A and B. Thromb Haemost. 2000;83:433-437.
7. Merskey C, Macfarlane RG. The female carrier of haemophilia. A clinical and laboratory study. Lancet. 1951;260:487-490.
8. Graham JB, Miller CH, Reisner HM, Elston RC, Olive JA. The phenotypic range of hemophilia A carriers. Am J Hum Genet. 1976;28:482-488.
9. Lusher JM, Mcmillan CW. Severe factor VIII and factor IX deficiency in females. Am J Med. 1978;65:637-648.
10. Mauser-Bunschoten EP, van Houwelingen JC, Sjamsoedin-Visser EJ, et al. Bleeding symptoms in carriers of haemophilia A and B. Thromb Haemost. 1988;59:349-352.
11. Wahlberg T. Carriers and noncarriers of haemophilia A. Evaluation of bleeding symptoms registered by a self-administered questionnaire with binary (no/yes) questions. Thromb Res. 1982;25:415-422.
12. Wahlberg T, Blomback M, Brodin U. Carries and noncarriers of haemophilia A: multivariate analysis of pedigree data, screening blood coagulation tests and factor VIII variables. Thromb Res. 1982;25:401-414.
13. Yang MY, Ragni MV. Clinical manifestations and management of labor and delivery in women with factor IX deficiency. Haemophilia. 2004;10:483-490.
14. Sramek A, Eikenboom JC, Briët E, Vandenbroucke JP, Rosendaal FR. Usefulness of patient interview in bleeding disorders. Arch Intern Med. 1995;155:1409-1415.
15. White GC, Rosendaal F, Aledort LM, et al. Definitions in hemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost. 2001;85:560.
16. Knobe KE, Ljung RCR. Haemophilia B carrier detection by factor IX:C analysis; no impact of the type of mutation or severity of disorder. Haemophilia. 1999;5:238-242.