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
ID
12739
Availability
Weekdays.
Additional Information
Haemostasis Consultant authorisation required. This test is performed by the Royal Hallamshire Hospital, Sheffield.
Turn Around
12 weeks.
Send To
Specialist Coagulation
Chancellor / Lincoln Wing Link Corridor
Pathology
Block 32
St James University Hospital
Beckett Street
Leeds
LS9 7TF
Contact
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.
Sample Req
Blood.
Ref Range Notes
Normal or abnormal binding.
Units
Descriptive Report.