VWD2 - von Willebrand's Disease Type II/Générique

Moderate to severe bleeding disorder

Description: 
Low level and abnormal function of von Willebrand factor, a protein involved in blood coagulation
Symptomes: 
Important bleedings or haemorrhagic episodes, potentially lethal, excessive gingival haemorrhage during eruption of adult teeth, nose bleeding, skin bruising, prolonged bleeding after surgery or trauma
Age d'aparition: 
From birth
Fréquence: 
Not available
Gène impliqué: 
VWF
Mutation testée: 
A>G in a2 domain
Transmission: 
Autosomal Recessive
Brevet: 
-