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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

Ref. Range (Male) Interpretative comment
Ref. Range (Female) Interpretative comment
Ref. Range (Paed) Interpretative comment
Ref. Range Notes
Units - Not Defined -

Other Help:National Laboratory Medicine Handbook

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. Last edited on 06/04/2019 15:24:37. Published By on 06/04/2018 15:24:37.