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...
Saved in:
Main Authors: | Ibrahim Abukhiran (Author), Judy Jasser (Author), Sharathkumar Bhagavathi (Author) |
---|---|
Format: | Book |
Published: |
Elsevier,
2020-11-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Education Case: Hereditary Thrombophilia With Double Heterozygous Factor V Leiden and Factor II c.*97G>A Mutations
by: Ibrahim Abukhiran MBBS, et al.
Published: (2021) -
Management of pregnancy and labor in female with combination of homozygous Leiden and heterozygous prothrombin G20210A mutations
by: M. O. Arslanbekova, et al.
Published: (2020) -
PREGNANCY AND CHILDBIRTH IN A YOUNG WOMAN WITH CONCOMITANT MUTATION IN LEIDEN AND PROTHROMBIN GENE G20210A
by: D. L. Kapanadze
Published: (2016) -
Factor-V Leiden G1691A and prothrombin G20210A polymorphisms in Sudanese women with preeclampsia, a case -control study
by: Nadir A. Ahmed, et al.
Published: (2019) -
Hereditary thrombophilia by factor V Leiden G1691A (heterozygous) and FII prothrombin G20210A (homozygous) mutations in a patient with ischemic cerebrovascular accident
by: Leonardo G. P. Ruiz, et al.
Published: (2018)