Novel compound heterozygous mutation of the KNG1 gene associated with severe HMWK deficiency in a Chinese pedigree
We report a novel compound heterozygous mutation (c.611C>T and c.718C>T) in the KNG1 gene causing severe HMWK deficiency. This case expands the mutational spectrum of this ultra-rare disorder and highlights that its primary clinical significance is an isolated APTT prolongation without a bleeding diathesis. Genetic diagnosis is crucial to avoid unnecessary treatments, surgical delays, and exposure to blood products in such patients.
Authors
- Bing Li
- Leonardo Brandao
- Xiaoying Fu
- Wei Liu
- Ying Wang
- Juan Huang
- Wujiao Li
- Weiwei Xiao
Institutions
- University of Toronto (CA)
- Hospital for Sick Children (CA)
- Public Health Ontario (CA)
- Shenzhen Children's Hospital (CN)
Publication Details
- Journal
- Blood Coagulation & Fibrinolysis
- Published
- 2026-03-12
- DOI
- https://doi.org/10.1097/mbc.0000000000001412
- Primary Topic
- Congenital Ear and Nasal Anomalies
- Type
- article
- Field-Weighted Citation Impact
- 0.00