Definite diagnosis of plasma prekallikrein deficiency should not be based exclusively on shortening of the aPTT upon prolonged pre‐incubation
- 4 April 2022
- journal article
- research article
- Published by Wiley in International Journal of Laboratory Hematology
- Vol. 44 (4) , e179-e180
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Prekallikrein deficiency due to homozygous KLKB1(+) mutation c.444_445insT (p.Ser151PhefsTer34)International Journal of Laboratory Hematology, 2021
- c.451dupT in KLKB1 is common in Nigerians, confirming a higher prevalence of severe prekallikrein deficiency in Africans compared to EuropeansJournal of Thrombosis and Haemostasis, 2020
- Severe plasma prekallikrein deficiency: Clinical characteristics, novel KLKB1 mutations, and estimated prevalenceJournal of Thrombosis and Haemostasis, 2020
- Severe prekallikrein deficiency due to a compound heterozygosis in the KLKB1-geneHamostaseologie, 2009
- High Molecular Weight Kininogen Deficiency: a Patient who Underwent Cardiac SurgeryThrombosis and Haemostasis, 2001