Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Clinical Impact of Inherited Thrombophilia in Patients With Thrombosis: Evaluating the Real Risk of FVL, PTG20210A, and MTHFR Mutations in the Kurdistan Region of Iraq.

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis - 1 Jan 2026

Abdulqader Aveen M Raouf, Noori Ahmed Sarwar, Noori Arya Sarwar, Mohammed Nazhad Hassan, Abdalla Heshw Salar, Mohammed Roman Salam, Mahmood Sarwar Noori

Abstract excerpt

BackgroundInherited thrombophilia, particularly Factor V Leiden (FVL) mutation, globally, stands as a known contributing factor for venous thromboembolism (VTE). However, there are minimal case-control studies about the genetic composition and risk of these mutations within the Kurdistan Region of Iraq (KRI). This study's goal was to analyze the frequency and clinical significance of FVL, Prothrombin G20210A, and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Case-Control Studies
Share to Factor V

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Prothrombin

Share to Thrombophilia

Share to Thrombosis

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 42544730
DOI: 10.1177/10760296261475425
PMCID: PMC13434878

Genes

MTHFR

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 17 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical Impact of Inherited Thrombophilia in Patients With Thrombosis: Evaluating the Real Risk of FVL, PTG20210A, and MTHFR Mutations in the Kurdistan Region of Iraq.PMID 42544730Read ↗

The Contributions of Thrombophilic Mutations to Genetic Susceptibility to Deep Venous Thrombosis in Iraqi Patients.Semantic proximity Read ↗

Frequency of genetic mutations associated with thromboembolism in the Western Black Sea Region.Semantic proximity Read ↗

Deep venous thrombosis and thrombophilic mutations in western Iran: association with factor V Leiden.Semantic proximity Read ↗

Prevalence of factor V leiden, MTHFR C677T and MTHFR A1298C polymorphisms in patients with deep vein thrombosis in Central Iran.Semantic proximity Read ↗

Association between factor V Leiden mutation and recurrent pregnancy loss in the middle east countries: a Newcastle-Ottawa meta-analysis.Semantic proximity Read ↗

Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians.Semantic proximity Read ↗

High prevalence of factor V Leiden and prothrombin G20101A mutations in Kashmiri patients with venous thromboembolism.Semantic proximity Read ↗

Maternal inherited thrombophilia and recurrent pregnancy loss: a Tunisian study and review of literature.Semantic proximity Read ↗

Genetic Risk Factors of Venous Thromboembolism in the East Algerian Population.Semantic proximity Read ↗

Factor V Leiden, prothrombin 20210G>A, MTHFR 677C>T and 1298A>C, and homocysteinemia in Tunisian blood donors.Semantic proximity Read ↗

FV Leiden mutation and risk of recurrent venous thromboembolism in Serbian population.Semantic proximity Read ↗

Prothrombin gene 20210A mutation in Slovak population.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.