Factor XII deficiency: case series on clinical manifestations and treatment approach

Factor XII deficiency or also known as Hageman factor deficiency is a rare inherited autosomal recessive coagulation disorder, attributed to mutation in F12 gene on chromosome 5. Affected individuals are mostly asymptomatic and diagnosed incidentally following pre-procedural assessment with finding...

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Bibliographic Details

Main Authors:	Jamhuri, Nur Syazwani, Ismail, Ilham, Pem, Tshering, Tumian, Nor Rafeah, Mahadi, Mahrunissa, Cheong, Xiong Kee, Chong, Guang Yong, Rodin, Nor Saaidah Kamal, Mohamad Azudin, Azhreen Fuad, Wan Hanafi, Hany Haqimi
Format:	Proceeding Paper
Language:	en en
Published:	John Wiley & Sons 2025
Subjects:	RC633 Specialties of Internal Medicines- Diseases of The Blood and Blood-forming Organs. Hematologic Diseases
Online Access:	http://irep.iium.edu.my/122348/1/122348_Factor%20XII%20deficiency.pdf http://irep.iium.edu.my/122348/2/Abstract%20Book%20EHA%202025.pdf http://irep.iium.edu.my/122348/ https://onlinelibrary.wiley.com/toc/25729241/2025/9/S1
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