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Pediatrics General 511110c0

The commonest mode of inheritance of Von Willebrand's diasease –

A
Codominant
B
Autosomal recessive
C
Autosomal dominant
D
X linked recessive
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.

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