VWD3-A - von Willebrand's Disease Type III/Scottish Terrier

Race liée: 

Severe bleeding disorder

Description: 
Lack of von Willebrand factor synthesis, a protein involved in blood coagulation
Symptomes: 
Important or severe bleeding disorders, difficult to contain, leading to death
Age d'aparition: 
From birth
Fréquence: 
15%
Gène impliqué: 
VWF
Mutation testée: 
c.264delC
Transmission: 
Autosomal Recessive
Brevet: 
_
Remarques: 
_