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Article

[Genetic variant C677T in the MTHFR in women with recurrent early fetal loss].

Akusherstvo i ginekologiia - 1 Jan 2007

Ivanov P, Kovacheva K, Komsa-Penkova R, Konova E, Simeonova M, Popov I, Gecheva S, Bozhinova S, Tanchev S, Tsafarov M

Abstract excerpt

The aim of this study was to evaluate correlation of carrier status for thrombophilic gene mutation--C677T in the methylenetetrahydrofolate reductase (MTHFR) and recurrent early pregnancy loss. Recently inherited thrombophilia was discussed as a predisposed factor for early recurrent fetal loss (ERFL). We investigated carrier status for C677T genetic variant in 54 women with ERFL before 10 week of gestation and...

Read the complete abstract on PubMed

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Share to Abortion, Habitual
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Polymorphism, Single Nucleotide

Share to Pregnancy

Share to Pregnancy Complications, Hematologic

Share to Thrombophilia

Source

Identifiers

PMID: 17974190

Genes

ERFL
MTHFR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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[Genetic variant C677T in the MTHFR in women with recurrent early fetal loss].PMID 17974190Read ↗

[A weak association of 677 C>T polymorphism in MTHFR with recurrent embryonic loss].Semantic proximity Read ↗

Association study between methylenetetrahydrofolate reductase polymorphisms and unexplained recurrent pregnancy loss: a meta-analysis.Semantic proximity Read ↗

MTHFR C677T polymorphism and recurrent early pregnancy loss risk in north Indian population.Semantic proximity Read ↗

Polymorphism for mutation of cytosine to thymine at location 677 in the methylenetetrahydrofolate reductase gene is associated with recurrent early fetal loss.Semantic proximity Read ↗

Methylenetetrahydrofolate reductase gene A1298C polymorphism and susceptibility to recurrent pregnancy loss: a meta-analysis.Semantic proximity Read ↗

[Genetic conditioned changes in activity of 5,10-methylenetetrahydrofolate reductase (MTHFR) and recurrent miscarriages].Semantic proximity Read ↗

[Genetic thrombophilic defects (Factor V Leiden, prothrombin G20210A, MTHFR C677T) in women with recurrent fetal loss].Semantic proximity Read ↗

Roles of methylenetetrahydrofolate reductase C677T polymorphism in repeated pregnancy loss.Semantic proximity Read ↗

Methylenetetrahydrofolate reductase gene polymorphisms in Egyptian women with unexplained recurrent pregnancy loss.Semantic proximity Read ↗

Association of MTR and MTRR polymorphisms with recurrent pregnancy loss: a case control study.Semantic proximity Read ↗

Association between maternal, fetal and paternal MTHFR gene C677T and A1298C polymorphisms and risk of recurrent pregnancy loss: a comprehensive evaluation.Semantic proximity Read ↗

A Pilot Study on Multigenic Thrombophilic Risk in Recurrent Pregnancy Loss: Interactions Between MTHFR Polymorphisms and Classical Thrombophilia-Associated SNPs.Semantic proximity Read ↗

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