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Hematopathology
Severe Prekallikrein Deficiency Associated with Low Level of Factor XII: A Case Report

Massoumeh Shahbazi; Minoo Ahmadinejad; Shahnaz Fakhrzadegan

Volume 16, Issue 3 , July 2021, , Pages 332-336

http://dx.doi.org/10.30699/ijp.2021.131638.2463

Abstract
  Hereditary deficiency of plasma prekallikrein (PPK) is a rare autosomal recessive disease. The affected patients are often asymptomatic and diagnosed incidentally during preoperative investigations or during hospitalization by isolated prolongation of activated partial thromboplastin time (aPTT). In ...  Read More