GENETIC RISK FACTORS ASSOCIATED WITH THROMBOSIS IN A SAMPLE OF IRAQ POPULATION
Keywords:
Abstract
Thrombosis is a complex disorder influenced by various genetic factors. This research paper aims to investigate the genetic risk factors associated with thrombosis in a sample of the Iraq population. Understanding the genetic determinants of thrombosis is crucial for early detection, prevention, and personalized treatment strategies. This study examines a sample of the Iraq population to identify specific genetic variations and polymorphisms that may contribute to an increased risk of thrombosis. Through genetic analysis techniques, such as polymerase chain reaction (PCR) and sequencing, the study explores the prevalence and potential impact of these genetic risk factors on thrombosis. The findings provide valuable insights into the genetic underpinnings of thrombosis in the Iraq population and may have implications for risk assessment, diagnosis, and targeted interventions.
Similar Articles
-
DANGERS OF DRUG ABUSE AMONG THE YOUTHS IN KEBBI STATE
The American Journal of Medical Sciences and Pharmaceutical Research: No. 07 (2023) / Abubakar Danjuma Bundaram , -
ANALYSIS OF THE THYROID STATUS OF PREGNANT WOMEN IN THE IODINE-DEFICIENT REGION
The American Journal of Medical Sciences and Pharmaceutical Research: No. 01 (2022) / Negmatova Gulzoda Shukhratovna, Togaeva Gulnora Siddiqovna, Davranova Aziza Davranovna, Azimbegova Sitora Nodirovna, -
Emergency Preparedness and Innovative Response Plan for Smooth Congregations during COVID-19 pandemic: An Urgent Need for Comprehensive Approaches to Tactically Resolve Risk of SARS-CoV-2 or MERS-CoV Transmission
The American Journal of Medical Sciences and Pharmaceutical Research: No. 11 (2021) / Umar Saeed , Zahra Zahid Piracha , Sara Rizwan Uppal , Muhammad Saad Uppal , Aftab Ahmad Khan , Muhammad Erfan Khattak, -
Extensively Drug Resistant Salmonella Enterica Serovar Typhi Misdiagnosis In Pakistan: A Matter Of Serious Concern
The American Journal of Medical Sciences and Pharmaceutical Research: No. 09 (2021) / Umar Saeed, Sara Rizwan Uppal , Zahra Zahid Piracha , Rizwan Uppal, -
UNVEILING THE CRISIS: THE GLOBAL CHALLENGE OF ANTIBIOTIC DRUG RESISTANCE
-
Microbiocenosis Of Open Cavities Of The Body
-
THE EFFECTIVENESS OF THE NEW SCHEME OF COMPLEX TREATMENT OF FRACTURES OF THE LOWER JAW
The American Journal of Medical Sciences and Pharmaceutical Research: No. 08 (2023) / Sh.N. Yakubov, K.E. Shomurodov, -
Effectiveness Of Domestic Preparation Kromoviz In Treatment Of Allergic Conjunctivites
The American Journal of Medical Sciences and Pharmaceutical Research: No. 06 (2021) / Nuraliev Nekkadam Abdullaevich, Safarov Jakhongir Oripovich, Khasanov Mukhriddin Khayotovich, -
DESIGN AND OPTIMIZATION OF EVEROLIMUS-LOADED PROTEIN NANOPARTICLES FOR TARGETED THERAPY OF GLIOBLASTOMAS
-
PECULIARITIES OF THE DEVELOPMENT OF ISCHAEMIC AND NON-ISCHAEMIC HEART DISEASE IN PATIENTS WITH RHEUMATOID ARTHRITIS (LITERATURE REVIEW)
References
Ali N, Hedyeh F T, Mohammad N, Sadaf T,Maryam J H, Fahimeh S T and Seyed R S(2013), “Screening for mutations in 10 exonsof the coagulation factor gene”, EuropeanJ.biology., Vol. 3, No. 3, pp. 589-592.
Asselta R and Peyvandi F (2009), Factor Vdeficiency SeminThrombHemost ., Vol. 35,No. 4, pp. 382-9.
Asselta R, Tenchini M L and Duga S (2006),“Inherited defects of coagulation factor V: thehemorrhagic side”, J.ThrombHaemost., Vol.4, No. 1, pp. 26-34.
Castoldi E, Simioni P, Kalafatis M, LunghiB, Tormene D, Girelli D, Girolami Aand Bernardi F (2000), “The prothrom-binase complex in a thrombophilic family”,Blood, Vol. 15, No. 4, pp. 1443-8.
Freeman W and Company H (2000).,Genetic Analysis, ISBN., 978(1):4180-5357.
Greer I A (2003), Best Pract Res Clin ObstetGynaecol., Vol. 17, No. 3, pp. 413-25.
Huang D D, Wang X F and Chen H Y (2010),“Analysis of phenotype and genotype in fourChinese pedigrees with inheritedcoagulation factor V deficiency”,ZhonghuaXue YeXueZaZhi, Vol. 31, p. 149.
Kumar and Vinay (2007), Robbins BasicPathology, Philadelphia: Saunders/Elsevier.ISBN: 978(1):4160-2973.
Lewis R (2004), Human Genetics:Concepts and Applications, 6th ed., McGrawHill. ISBN., 0072951745.
Ossowski S, Schneeberger K and Lucas-Lledó J I (2010), “The rate and molecularspectrum of spontaneous mutations”,Science., Vol. 1, No. 5961, pp. 92-4.
Press R D, Bauer K A, Kujovich J L, Heit J A(2002), Arch Pathol Lab Med., Vol. 126, No.11, pp. 1304-18.
