Coagulation Factor V Deficiency: Two Case Reports With a review of Literature.
DOI:
https://doi.org/10.21649/akemu.v4i4.4017Keywords:
Factor V, Coagulation defects, clotting factors.Abstract
Factor V deficiency is a very rare autosomal recessive trait. Commonest mode of presentation is bleeding from mucous membrane in the form of epistaxis or menorrhagia, later may be so severe as to be life threatening. We received two cases of factor V deficiency at the Pathology Department. of King Edward Medical College, Lahore. One child from paeditric surgery department. and other from Lady Willingdon Hospital, Lahore. Both were investigated, all the tests were normal but prothrombin time and activated partial thromboplastin time was prolonged which was corrected with adsorbed plasma. The diagnosis was confirmed by factor V assay.Published
How to Cite
Issue
Section

This work is licensed under a Creative Commons Attribution 4.0 International License.
This is an open-access journal and all the published articles / items are distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. For comments jspark@kemu.edu.pk