Literature DB >> 22897698

Prevalence of beta-thalassemia trait and abnormal hemoglobins in the province of Adıyaman, Turkey.

Ahmet Genc1, Deniz Tastemir Korkmaz, Meral Urhan Kucuk, Eyup Rencuzogullari, Selman Atakur, Suleyman Bayram, Muhittin Onderci, Tuba Koc, Sinan Aslan, Abdullah Mutalip, Muslum Faruk, Yusuf Sevgiler, Aygul Tuncdemir.   

Abstract

BACKGROUND/AIMS: Thalassemia is one of the most common hereditary disorders in Turkey. The aim of this study was to determine the prevalence of the beta-thalassemia trait and abnormal hemoglobins in the province of Adıyaman in Turkey.
METHODS: The study included 3571 high school students of both sexes; aged 12-22 (mean 16.59 ± 1.34). After they received information about thalassemia, they were screened for beta-thalassemia and abnormal hemoglobin using complete blood count (CBC) and quantification of hemoglobin. Hemoglobin was fractionated using HPLC.
RESULTS: The beta-thalassemia trait was found in 38 students (1.06%), and abnormal hemoglobin in seven students (0.20%). Of the latter, four carried HbD Los Angeles, two HbS, and one HbE-Saskatoon.
CONCLUSION: The prevalence of the beta-thalassemia trait and abnormal hemoglobin in the province of Adıyaman is low, compared to the rest of Turkey. Our results seem to reflect the heterogeneity of beta-thalassemia in the province of Adıyaman and may be of value for genetic counseling and premarital screening.

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Year:  2012        PMID: 22897698     DOI: 10.3109/08880018.2012.713085

Source DB:  PubMed          Journal:  Pediatr Hematol Oncol        ISSN: 0888-0018            Impact factor:   1.969


  1 in total

1.  An updated review of abnormal hemoglobins in the Turkish population.

Authors:  Nejat Akar
Journal:  Turk J Haematol       Date:  2014-03-05       Impact factor: 1.831

  1 in total

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