2000
DOI: 10.1055/s-0037-1613816
|View full text |Cite
|
Sign up to set email alerts
|

Thrombophilic Mutations in Iran

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
10
2

Year Published

2004
2004
2010
2010

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 15 publications
(12 citation statements)
references
References 7 publications
0
10
2
Order By: Relevance
“…The prevalence of prothrombin G20210A mutation in the present study was 1.6%, with allele frequency of 0.8%, which again, is lower than that found (3.1%, allele frequency of 1.5%) in Tehran population [10]. The prothrombin G20210A mutation is rarely seen in Asian populations [8].…”
Section: Discussioncontrasting
confidence: 81%
See 2 more Smart Citations
“…The prevalence of prothrombin G20210A mutation in the present study was 1.6%, with allele frequency of 0.8%, which again, is lower than that found (3.1%, allele frequency of 1.5%) in Tehran population [10]. The prothrombin G20210A mutation is rarely seen in Asian populations [8].…”
Section: Discussioncontrasting
confidence: 81%
“…The reasons for different prevalence of this thrombophilic mutation in our study, compared to Zeinali et al report [10], could be attributed to differences in sample sizes, differences in ethnic backgrounds and selection of the populations studied. Further, the allele frequency of factor V leiden mutation in our population is lower than some neighboring countries, including Turkey (4.5-4.9%) [14].…”
Section: Discussioncontrasting
confidence: 76%
See 1 more Smart Citation
“…Furthermore, Otrock et al [5] found that the concomitant presence of homozygosity for FV Leiden and heterozygosity for the methylenetetrahydrofolate reductase (MTHFR) mutation in a sickle-beta zero thalassemia patient led to the development of extensive deep vein thrombosis. A relatively high frequency of factor V Leiden mutation and a moderate frequency of prothrombin G20210A has been reported in Iranians [15]. Recently we studied 434 individuals from Western Iran and found a prevalence of 1.6% and 2.97% for prothrombin gene mutation and factor V Leiden, respectively (J Thromb Thrombolys, accepted for publication), which are lower than those from the prevalence of 5.5% for factor V Leiden and 3.1% for prothrombin mutation reported by Zeinali et al [15] in 161 subjects from Tehran, a city with mixed ethnicity.…”
Section: Discussionmentioning
confidence: 99%
“…The prevalence rate of 3% in Iraqi blood donors, although it is much lower than the prevalence rates of 14.2%, 13.6%, and 12.25% reported in Lebanon, Syria, and Jordan, respectively (4,7 ), and to a lesser extent than the rates in Turkey (7.4%) (8 ) and Iran (5.5%) (9 ), is comparable to the prevalence of 2.5% reported in Clinical Chemistry 50, No. 3, 2004 Saudi Arabia (10 ).…”
Section: To the Editormentioning
confidence: 71%