AI Article Synopsis

  • This study focuses on a significant case of a large genital hematoma following delivery, linked to a genetic mutation known as fibrinogen Dorfen.
  • Fibrinogen Dorfen involves a specific mutation in the fibrinogen protein that affects its structure and function, particularly impacting the polymerization process crucial for blood clotting.
  • Despite both the patient and her mother carrying the same genetic mutation, their clinical outcomes varied significantly, highlighting the need to investigate how differences in fibrinogen function can lead to diverse perinatal results.

Article Abstract

This study demonstrates a case of a huge genital hematoma after delivery, associated with fibrinogen Dorfen. Fibrinogen Dorfen is the mutation of a fibrinogen-coded exon gene, which has a single heterozygous GCC → GTC transition at codon 289 of the γ gene, predicting an Ala → Val substitution. Because Ala289 plays a crucial role in maintaining the structure of the polymerization site of hole 'a' via a hydrogen bond, it is speculated that the γ 289Ala → Val substitution can change not only the fibrinogen structure, but also the function of polymerization. In our case, although the patient's gene mutation was the same as that of her mother, there was a discrepancy in the clinical outcomes. Although the precise mechanism regarding this discrepancy remains unknown, it may cause different perinatal outcomes in terms of vaginal delivery, such as the severe bleeding in this patient and the absence of clinical symptoms in her mother. This is the first report suggesting the heterogeneity of fibrinogen functions of fibrinogen Dorfen, which may be critical to the clinical outcome.

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Source
http://dx.doi.org/10.1111/jog.12972DOI Listing

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