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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. As a result the T of FVIII is significantly reduced as it is no longer protected from proteolytic degradation within the plasma.
Indication vWD subtyping
Additional Info Haemostasis Consultant authorisation required. This test is performed by the Royal Hallamshire Hospital, Sheffield.
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 NotesReported as normal or abnormal binding.
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 CommentReferred Test - Royal Hallamshire Hospital, Sheffield
Originally edited by : Chris Wilks. Last edited on 21/05/2022 10:19:11. Published By Brad Dickinson on 21/05/2020 10:19:11.