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Published on: August 17, 2022
[Mutation analysis and prenatal diagnosis for a family affected with congenital factor VII deficiency]
Wei Peng1, Shuxin Zhang, Xin Liu
1Developmental Biology Laboratory, Bayi Children's Hospital Affiliated to Beijing Military Region General Hospital, Beijing 100700, China. 001wangyan@sina.com.
Objective:
To provide mutation analysis and prenatal diagnosis for a family affected with congenital factor VII(FVII) deficiency.
Methods:
DNA was extracted from peripheral blood samples from the proband and his parents. All exons and flanking sequence of the FVII gene were amplified with PCR and subjected to direct sequencing. Prenatal diagnosis was performed by amniocentesis.
Results:
A homozygous mutation (NM_000131.3) c.572-1G>A was identified in the proband. Both parents of the fetus were carriers of the mutation.
Conclusion:
A method for molecular diagnosis of congenital factor VII deficiency was established and successfully applied for an affected family.
