Hereditary combined deficiency of vitamin K–dependent clotting factors presenting as postoperative haemorrhage in a Syrian adolescent: a likely VKCFD type 2 phenotype
Consider vitamin K-dependent clotting factors deficiency in unexplained prolonged prothrombin time/activated partial thromboplastin time with normal vitamin K and combined factor deficiencies.Early recognition prevents catastrophic bleeding; vitamin K and factor replacement are lifesaving.Internists play a pivotal role in differentiating inherited from acquired coagulopathies.
Authors
- Mahmoud Alhamadeh Alswij (ORCID: https://orcid.org/0000-0003-0607-0889)
- Anas Alyousef (ORCID: https://orcid.org/0000-0002-5450-8083)
- Mais Musleh (ORCID: https://orcid.org/0000-0002-2148-2921)
- Nighat Mir Ahmad
- Abdullatif AlStem
- Hadi Ataya
Institutions
- Damascus Hospital (SY)
- Al Wataniya Private University (SY)
- Al Assad University Hospital (SY)
- Damascus University (SY)
Publication Details
- Journal
- European Journal of Case Reports in Internal Medicine
- Published
- 2025-11-10
- DOI
- https://doi.org/10.12890/2025_005928
- Primary Topic
- Vitamin K Research Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00