[Home ] [Archive]   [ فارسی ]  
:: Main :: About :: Current Issue :: Archive :: Search :: Submit :: Contact ::
Main Menu
Home::
Journal Information::
Indexing Databases::
Editorial Board::
Executive Members::
Instruction to Authors::
Peer Review::
Articles Archive::
Contact Us::
Site Facilities::
::
Search in website

Advanced Search
Receive site information
Enter your Email in the following box to receive the site news and information.
:: Volume 15, Issue 4 (12-2013) ::
J Gorgan Univ Med Sci 2013, 15(4): 79-83 Back to browse issues page
Chromosomal aberrations in patients suspected with the risk of Fanconi anemia
Rezamand A1 , Asghari Estiar M2 , Sadeghi B3 , Sakhinia E *4
1- Assistant Professor, Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
2- MSc Student of Medical Genetics, Scientific Research Center, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
3- MSc in Laboratory Sciences, Tabriz Genetic Analysis Center (TGAC), Tabriz University of Medical Sciences, Tabriz, Iran
4- Associate Professor, Tuberculosis and Lung Disease Research Center, Tabriz University of Medical Sciences, Tabriz, Iran , esakhinia@yahoo.co.uk
Abstract:   (15104 Views)
Background and Objective: Fanconi anemia is the most prevalent inherited aplastic anemia. Diagnosis based solely on the recognition of clinical symptoms is not reliable. This study was done to determine chromosomal aberrations in patients suspected with the risk of Fanconi anemia in the Eastern Azarbaijan province- Iran. Materials and Methods: This descriptive study was conducted on 20 patients in the Eastern Azarbaijan province-Iran. The cytogenetic method was used to determine type and number of chromosomal disorders. Results: Nine eight and nine patients had co-morbid anemia, platelet deficiency and 9 patients had hand and finger deformities, respectively. Using cytogenetic method, Fanconi anemia was confirmed in 5 (25%) of the cases. The percentage of mitotic abnormalities in the chromosomes without administration of mitomycin C varied between 5-30% in the cultures of the 5 affected and between 0-4% in the 15 unaffected patients with the administration of mitomycin C, the percentages were increased up to 35-78% and 0-20% in affected and unaffected patients, respectively. Conclusion: Fanconi anemia is confirmed precisely in 25% of suspected patients using cytogenetic method.
Keywords: Fanconi anemia, Chromosomal breakage, Mitomycin C
Full-Text [PDF 295 kb] [English Abstract]   (25567 Downloads)    
Type of Study: Original Articles | Subject: Hematology
Send email to the article author


XML   Persian Abstract   Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Rezamand A, Asghari Estiar M, Sadeghi B, Sakhinia E. Chromosomal aberrations in patients suspected with the risk of Fanconi anemia. J Gorgan Univ Med Sci 2013; 15 (4) :79-83
URL: http://goums.ac.ir/journal/article-1-1879-en.html


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 15, Issue 4 (12-2013) Back to browse issues page
مجله دانشگاه علوم پزشکی گرگان Journal of Gorgan University of Medical Sciences
Persian site map - English site map - Created in 0.06 seconds with 34 queries by YEKTAWEB 4710
Creative Commons License
This work is licensed under a Creative Commons — Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)