Author:
Green PP,Mannucci PM,Briet E,Ljung R,Kasper CK,Essien EM,Chediak J,Rizza CR,Graham JB
Abstract
Abstract
Factor VIII (F.VIII) and von Willebrand factor (VWF):Ag data collected by eight laboratories on a total of 336 obligatory carriers of hemophilia A and 137 normal women were used to answer several questions concerning the construction of linear discriminants for carrier detection. It was found: that a “universal” linear discriminant can be constructed which is suitable for use in all laboratories and is nearly as effective as laboratory-specific discriminants; that inclusion of age and ABO blood type data improved the efficacy of these discriminants; that substitution of alternative assays for F.VIII and VWF:Ag did not generally improve the efficacy of the discriminants over that obtained using the bioassay for F.VIII:C and Laurell's immunoassay for VWF:Ag; that linear discriminants were far more effective than discriminants based on the F.VIII:C/VWF:Ag ratio. A step-wise procedure is given which any laboratory may follow in using the universal discriminant for carrier detection.
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Cited by
25 articles.
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2. ABO Blood Groups and Cardiovascular Diseases;International Journal of Vascular Medicine;2012
3. Hemophilia A;Atlas of Genetic Diagnosis and Counseling;2012
4. Coagulation and Fibrinolysis;Henry's Clinical Diagnosis and Management by Laboratory Methods;2011
5. Carrier detection strategy in haemophilia A: the benefits of combined DNA marker analysis and coagulation testing in sporadic haemophilic families;British Journal of Haematology;2008-07-07