Double-homozygosity for Factor V Leiden and Prothrombin c.*97G > A Mutation in a Young Female with Recurrent Fetal Losses and no Venous Thromboembolism

Double-homozygosity for Factor V Leiden and Prothrombin c.*97G > A Mutation in a Young Female with Recurrent Fetal Losses and no Venous Thromboembolism

Factor V Leiden (FVL) and factor II c.*97G > A mutation are the two most common genetic factors predisposing to hereditary thrombophilia. Being extremely rare, it used to be thought that double homozygosity for both variants is inconsistent with life. Only two cases describing double-homozygous p...

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Bibliographic Details
Main Authors: Ibrahim Abukhiran, Judy Jasser, Sharathkumar Bhagavathi
Format: Article
Language:English
Published: Elsevier 2020-11-01
Series:Human Pathology: Case Reports
Subjects:
Factor V Leiden
FVL
Factor II
c.*97G>A
Mutation
Double-homozygosity
Online Access:http://www.sciencedirect.com/science/article/pii/S2214330020300742

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