AI Article Synopsis

  • Many African Americans with factor VII (FVII) deficiency show no symptoms, but the genetic causes of this condition have not been studied before.
  • Research on three unrelated patients revealed that a specific nucleotide change led to a mutation that impacts FVII levels in lab tests.
  • Understanding this genetic defect can help healthcare professionals better interpret lab results and avoid unnecessary blood transfusions for patients with abnormal readings.

Article Abstract

African Americans with factor VII (FVII) deficiency, as defined by clinical laboratory values, are frequently asymptomatic. To date the genotypes underlying this FVII defect in asymptomatic African Americans have not been established. We show in 3 unrelated African-American patients that the defect is due to a G to A nucleotide change resulting in an arginine to glutamine mutation in Factor VII amino acid 304. This defect results in low FVII coagulant activity levels using rabbit brain thromboplastin but not using human thromboplastin. This report may aid transfusion and hematology specialists evaluate patient results and prevent unnecessary transfusions to treat patients with abnormal laboratory values.

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Source
http://dx.doi.org/10.1309/36HQ-36ET-U7K8-MUXTDOI Listing

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