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L. Baronciani

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Open access Mar 2011

Clinical, Laboratory, and Molecular Markers of Type 3 von Willebrand Disease

Type 3 von Willebrand disease (VWD3) is due to a virtually complete deficiency of von Willebrand factor (VWF), and it is inherited as an autosomal recessive trait: heterozygous relatives have mild or no bleeding symptoms. The prevalence of VWD3 is very low, ranging from 0.1 to 5.3 per million population. VWD3 patients...

L. Baronciani, A. Federici, J. Eikenboom · 5 citations

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