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Type 3 von Willebrand disease (VWD) is a rare autosomal recessive disorder characterized by undetectable von Willebrand Antigen (VWF:Ag). Carriers of type 3 VWD carry one null allele and have… Click to show full abstract
Type 3 von Willebrand disease (VWD) is a rare autosomal recessive disorder characterized by undetectable von Willebrand Antigen (VWF:Ag). Carriers of type 3 VWD carry one null allele and have von Willebrand factor (VWF) at about 50% of normal. The aim of this study was to characterize type 3 VWD carriers and to study the role of Platelet Function Analyzer (PFA‐200) in this cohort.
Keywords:
willebrand;
willebrand disease;
von willebrand;
role platelet;
carriers type;
type von
Journal Title: International Journal of Laboratory Hematology
Year Published: 2022
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Journal Title: International Journal of Laboratory Hematology
Year Published: 2022
Link to full text (if available)
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recommendations!