Yerevan
EN
Lab tests
42-126

Molecular genetic analysis for von Willebrand disease types 1, 2A, 2B, 2M, 2N, 3 (VWF gene exons 18-21 and 28)

Description

Von Willebrand disease is one of the most common genetically determined blood coagulation disorders. The disease is caused by aberrations in the VWF gene, which encodes the von Willebrand factor. Depending on the pathological changes in the von Willebrand factor, disease types are distinguished by quantitative changes (Type 1 and Type 3) and qualitative changes (Type 2A, 2B, 2M, 2N).

Period of execution

Within 12 days. The specified time does not include the day of biomaterial collection

Biomaterial type

  • Venous blood
Total price
65965 ֏
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