Article
Genotypes of European and Iranian patients with type 3 von Willebrand disease enrolled in 3WINTERS-IPS.
Blood advances - 10 Aug 2021
Baronciani Luciano, Peake Ian, Schneppenheim Reinhard, Goodeve Anne, Ahmadinejad Minoo, Badiee Zahra, Baghaipour Mohammad-Reza, Benitez Olga, Bodó Imre, Budde Ulrich, Cairo Andrea, Castaman Giancarlo, Eshghi Peyman, Goudemand Jenny, Hassenpflug Wolf, Hoorfar Hamid, Karimi Mehran, Keikhaei Bijan, Lassila Riitta, Leebeek Frank W G, Lopez Fernandez Maria Fernanda, Mannucci Pier Mannuccio, Marino Renato, Nikšić Nikolas, Oyen Florian, Santoro Cristina, Tiede Andreas, Toogeh Gholamreza, Tosetto Alberto, Trossaert Marc, Zetterberg Eva M K, Eikenboom Jeroen, Federici Augusto B, Peyvandi Flora
Abstract excerpt
Type 3 von Willebrand disease (VWD3) is a rare and severe bleeding disorder characterized by often undetectable von Willebrand factor (VWF) plasma levels, a recessive inheritance pattern, and heterogeneous genotype. The objective of this study was to identify the VWF defects in 265 European and Iranian patients with VWD3 enrolled in 3WINTERS-IPS (Type 3 Von Willebrand International Registries Inhibitor...
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