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ID:1043 Von Willebrands Normandy Screen
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Description 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.
Indication vWD subtyping
Additional Info Haemostasis Consultant authorisation required
Concurrent TestsvW Screen
Dietary Requirementsna
Interpretation Interpretative comment

DepartmentSpecialist Laboratory Medicine
SampleBlood
TubeCoagulation
Tube Picture
Collection Conditions
Min. Vol
Freq.

Ref. Range (Male) Interpretative comment
Ref. Range (Female) Interpretative comment
Ref. Range (Paed) Interpretative comment
Ref. Range Notes
Units - Not Defined -
IP Acute TAT- Not Defined -
IP Routine TAT3 months
GP Acute TAT- Not Defined -
GP Routine TAT- Not Defined -
Turnround CommentNA

Originally edited by : Chris Wilks. Review due on 06/04/2019 15:24:37. Published By on 06/04/2018 15:24:37.