The commonest mode of inheritance of Von Willebrand's diasease –
High-Yield Explanation
Von Willebrand disease
Von Willibrand disease is of following types -
1)Type I (most common 70%) → Autosomal dominant, with reduced quantity of vWF.
2)Type II (25%) → Autosomal dominant, with qualitative defect of vWF.
3)Type II → Autosomal recessive, with reduced quantity of vWF.