AUTHOR=Chang Yueh-Shih , Lan Yi-Cheng , Chen Ya-Jyun , Huang Jen-Seng , Yang Chia-Ning , Huang Chi-Ying F. , Yeh Kun-Yun 

TITLE=A Novel Phenotype of the Factor 5 Gene Mutation (Homozygote Met1736Val and Heterozygote Asp68His) Is Associated With Moderate Factor V Deficiency

JOURNAL=Frontiers in Medicine

VOLUME=9

YEAR=2022

URL=https://www.frontiersin.org/journals/medicine/articles/10.3389/fmed.2022.870269

DOI=10.3389/fmed.2022.870269

ISSN=2296-858X

ABSTRACT=<sec><title>Background</title><p>Factor V (FV) deficiency is a rare disease, with a low incidence rate in Asia. Therefore, the <italic>F5</italic> mutation in the Taiwanese population is poorly understood.</p></sec><sec><title>Methods</title><p>A Chinese family with FV deficiency was included, and the patient and his family members underwent mutation analysis. Then, patients from Keelung City (Taiwan) were screened for <italic>F5</italic> polymorphism; the Chang Gung Human Database was used to determine single-nucleotide variants in the non-FV-deficient patient population.</p></sec><sec><title>Results</title><p>Eight mutation sites on the <italic>F5</italic> gene locus, including exon 16 homozygote Met1736Val and seven heterozygous mutations, including Asp68His, were found. Moreover, Met1736Val was found to be the dominant mutation in people living in the Taiwan community, and this result was compared with the records of the Chang Gung Human Database. The above-mentioned polymorphisms may result in a variable incidence of FV deficiency in Keelung City, thereby facilitating carrier diagnosis and prenatal diagnosis in most FV-deficient families.</p></sec><sec><title>Conclusion</title><p>The homozygote Met1736Val and the co-inheritance of the Asp68His <italic>F5</italic> gene are unique and worthy of screening in FV-deficient patients.</p></sec>