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Article

Undetected factor VIII in a patient with type 3 von Willebrands disease mistaken as severe haemophilia A.

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Nov 2009

Mullah-Ali A M, Chan A K, Lillicrap D, Decker K, Seroski W, Moffat K, Walker I, Pai M K

Abstract excerpt

von Willebrand disease (VWD) type 3 is a rare disorder characterized by absent or <0.1 UmL(-1) of ristocetin cofactor (VWF:RCo), and a very low level of factor VIII (FVIII:C). A total absence of FVIII:C has never been reported in type 3 VWD. This case illustrates the effect of severe von Willebrand factor (VWF) deficiency on the factor VIII level.

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Source

Identifiers

PMID: 19563498
DOI: 10.1111/j.1365-2516.2009.02062.x

Genes

VWF

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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