Von Willebrands Normandy Screen
Type 2N [Normandy] VWD is a recessively inherited disorder due to a mutation in von Willebrand Factor that impairs its ability to bind to and transport FVIII in the plasma.
|Tube||05 (CP) - Citrate|
|Additional Information||Haemostasis Consultant authorisation required. This test is performed by the Royal Hallamshire Hospital, Sheffield.|
|Turn Around||90 days|
|Send to||Specialist Coagulation
Chancellor / Lincoln Wing Link Corridor
St James University Hospital
|Collection Con||2 x citrate samples (all citrate tubes must be filled to the line).
Samples must be processed within 6 hours of being taken.
|Ref. Range Notes||Normal or abnormal binding.