Cargando…

MTHFR C677T, Prothrombin G20210A, and Factor V Leiden (G1691A) Polymorphism and Beta-Thalassemia Risk: A Meta-Analysis

Background Beta (β)-thalassemia major patients frequently suffer from many vascular problems. Thrombophilia is a blood disorder that comprises imbalances in the blood coagulating factor due to ecological and hereditary components. Previous evidence shows that thrombosis is the commonest risk in beta...

Descripción completa

Detalles Bibliográficos
Autores principales:	Nigam, Nitu, Singh, Prithvi K, Agrawal, Monica, Nigam, Sanjay, Gupta, Harish, Saxena, Shailendra
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Cureus 2020
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603879/ https://www.ncbi.nlm.nih.gov/pubmed/33150118 http://dx.doi.org/10.7759/cureus.10743

Ejemplares similares

Large‐scale screening for factor V Leiden (G1691A), prothrombin (G20210A), and MTHFR (C677T) mutations in Greek population
por: Raptopoulou, Alkistis, et al.
Publicado: (2022)

Factor V Leiden G1691A and Prothrombin Gene G20210A Mutations on Pregnancy Outcome
por: Padda, Jaskamal, et al.
Publicado: (2021)

The Role of Factor V Leiden, Prothrombin G20210A, and MTHFR C677T Mutations in Neonatal Cerebral Sinovenous Thrombosis
por: Garrido-Barbero, Maria, et al.
Publicado: (2019)

Factor V Leiden G1691A and prothrombin G20210A mutations among Palestinian patients with sickle cell disease
por: Samarah, Fekri, et al.
Publicado: (2018)

Factor-V Leiden G1691A and prothrombin G20210A polymorphisms in Sudanese women with preeclampsia, a case -control study
por: Ahmed, Nadir A., et al.
Publicado: (2019)

Frequency and association of 1691 (G>A) FVL, 20210 (G>A) PT and 677 (C>T) MTHFR with deep vein thrombosis in the population of Bosnia and Herzegovina
por: Jusić-Karić, A, et al.
Publicado: (2016)

Thrombophilic Risk of Factor V Leiden, Prothrombin G20210A, MTHFR, and Calreticulin Mutations in Essential Thrombocythemia Egyptian Patients
por: El-Ghonemy, Mohamed S., et al.
Publicado: (2020)

Prevalence of Factor V Leiden G1691A and Prothrombin G20210A Gene Mutation Among Pregnant Women: Experience from a Multi-Center Study in Nigeria
por: John-Olabode, Sarah O, et al.
Publicado: (2021)

Direct‐to‐consumer genetic testing for factor V Leiden and prothrombin 20210G>A: the consumer experience
por: Elson, Sarah L., et al.
Publicado: (2020)

A Hypertrophic Spinal Pachymeningitis Patient With Factor V Leiden (G1691A), MTHFR C677T, MTHFR A1298C, PAI-1 4G-5G, Glycoprotein IIIa L33P Gene Mutations
por: Civlan, Serkan, et al.
Publicado: (2022)

Acute Myocardial Infarction in Patients with Hereditary Thrombophilia—A Focus on Factor V Leiden and Prothrombin G20210A
por: Badescu, Minerva Codruta, et al.
Publicado: (2023)

The Combined Heterozygosity of Factor V Leiden and G20210A Prothrombin Gene Mutation in a Patient With Venous Thromboembolism
por: Machado, Marcia, et al.
Publicado: (2023)

The role of FV 1691G>A, FII 20210G>A mutations and MTHFR 677C>T; 1298A>C and 103G>T FXIII gene polymorphisms in pathogenesis of intraventricular hemorrhage in infants born before 32 weeks of gestation
por: Szpecht, Dawid, et al.
Publicado: (2017)

PlA2 Polymorphism of Platelet Glycoprotein IIb/IIIa and C677T Polymorphism of Methylenetetrahydrofolate Reductase (MTHFR), but Not Factor V Leiden and Prothrombin G20210A Polymorphisms, Are Associated with More Severe Forms of Legg–Calvé–Perthes Disease
por: García-Alfaro, María Dolores, et al.
Publicado: (2021)

Risk of Budd-Chiari Syndrome Associated with Factor V Leiden and G20210A Prothrombin Mutation: A Meta-Analysis
por: Zhang, Peijin, et al.
Publicado: (2014)

Association of Factor V Leiden and Prothrombin G20210A Polymorphisms in Women with Recurrent Pregnancy Loss in Isfahan Province, Iran
por: Kardi, Mohammad Taghi, et al.
Publicado: (2018)

Epidemiology of Prothrombin G20210A Mutation in the Mediterranean Region
por: Jadaon, Mehrez M.
Publicado: (2011)

Factor V Leiden and Prothrombin 20210A Mutations among Turkish Pediatric Leukemia Patients
por: Akın, Dilara Fatma, et al.
Publicado: (2012)

Evaluation of Gestational Diabetes Mellitus Risk in South Indian Women Based on MTHFR (C677T) and FVL (G1691A) Mutations
por: Khan, Imran Ali, et al.
Publicado: (2015)

The impact of prothrombin (G20210A) gene mutation on stroke in youths
por: Saadatnia, Mohammad, et al.
Publicado: (2012)

Prevalence of the prothrombin G20210A mutation among ischemic stroke patients
por: Ahmed, Salar A., et al.
Publicado: (2020)

Mutation in the Prothrombin Gene G20210A as a Cause of Cerebral Venous Thrombosis
por: Arroyave, Jorge A., et al.
Publicado: (2012)

Painless Livedoid Vasculopathy in a Patient with G20210A Prothrombin Gene Mutation
por: Mirrakhimov, Aibek E., et al.
Publicado: (2012)

Pregnancy complications in G20210A mutation carriers associated with high prothrombin activity
por: Nikolaeva, M. G., et al.
Publicado: (2021)

Thrombophilic Genetic Factors PAI-1, MTHFRC677T, V Leiden 506Q, and Prothrombin 20210A in Noncirrhotic Portal Vein Thrombosis and Budd-Chiari Syndrome in a Caucasian Population
por: D'Amico, Mario, et al.
Publicado: (2013)

Factor VLeiden and Prothrombin G20210A Gene Polymorphisms in Patients with Coronary Artery Disease
por: Ercan, Bahadır, et al.
Publicado: (2008)

Genetic correlation between Prothrombin G20210A polymorphism and retinal vein occlusion risk
por: Zou, Yuanyuan, et al.
Publicado: (2019)

Prothrombin Gene G20210A Variant in Angiographically Documented Patients with Coronary Artery Stenosis
por: Pourgholi, Leyla, et al.
Publicado: (2019)

Association of G20210A Prothrombin Gene Mutation and Cerebral Ischemic Stroke in Young Patients
por: Poudel, Sujan, et al.
Publicado: (2020)

Cerebral venous sinus thrombosis in heterozygous prothrombin G20210A mutation in Egyptian child, with an excellent outcome
por: Attia, Tarek Hamed, et al.
Publicado: (2015)

Factor V Leiden, Prothrombin and MTHFR Mutation in Patients with Preeclamsia, Intrauterine Growth Restriction and Placental Abruption
por: Livrinova, Vesna, et al.
Publicado: (2015)

Factor V Leiden 1691G > A mutation and the risk of recurrent pregnancy loss (RPL): systematic review and meta-analysis
por: Eslami, Mohammad Masoud, et al.
Publicado: (2020)

Altered pro-inflammatory and anti-inflammatory plasma cytokines levels in children with Down's syndrome: A meta-analysis
por: Nigam, Nitu, et al.
Publicado: (2021)

Prothrombin Gene G20210A Mutation in Acute Deep Venous Thrombosis Patients with Poor Response to Warfarin Therapy
por: Attia, F.M, et al.
Publicado: (2009)

Cerebral Venous Sinus Thrombosis with Bilateral Abducens Palsy in a Patient with Heterozygous Prothrombin G20210A Mutation
por: Sodavarapu, Soujanya, et al.
Publicado: (2019)

Case control study of the factor V Leiden and factor II G20210A mutation frequency in women with recurrent pregnancy loss
por: Teremmahi Ardestani, Majid, et al.
Publicado: (2013)

Allele frequency distribution of 1691G>A F5 (which confers Factor V Leiden) across Europe, including Slavic populations
por: Clark, Jeremy S. C., et al.
Publicado: (2013)

A demographic prevalence of β Thalassemia carrier and other hemoglobinopathies in adolescent of Tharu population
por: Nigam, Nitu, et al.
Publicado: (2020)

Different outcome of six homozygotes for prothrombin A20210A gene variant
por: Di Micco, Pierpaolo, et al.
Publicado: (2008)

Prevalence and Geographical Variation of Prothrombin G20210A Mutation in Patients with Cerebral Vein Thrombosis: A Systematic Review and Meta-Analysis
por: Gonzalez, Joaquín V., et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_mo8o4f1gdk556cpvj9ljqpeqvi