Prevalence and Distribution of Thalassemia Trait Screening
نویسندگان
چکیده
منابع مشابه
Prevalence of Beta Thalassemia Trait in Denizli.
Beta thalassemia, characterized by the deficiency or the absence of beta globulin production, is the most widespread inherited disorder in the world and is also common in Turkey. To determine the prevalence of carriers for beta thalassemia, we screened the couples before their marriage. For this aim, from 1994 to 1999, a total of 14.200 people were screened. The complete blood count and red blo...
متن کامل'NESTROFT'--an effective screening test for beta thalassemia trait.
OBJECTIVE To evaluate the efficacy of NESTROFT (Naked Eye Single Tube Red Cell Osmotic Fragility Test) as a screening tool for detection of beta thalassemia trait. DESIGN Prospective study. SETTING Field camps in various parts of Gujarat and Maharashtra States. METHODS A total of 2525 subjects were screened. NESTROFT, complete hemogram including red cell indices and calculation of Mentzer...
متن کاملPrevalence and mutations of β-thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province, Turkey
The prevalence of β-thalassemia (β-thal) carriers in Turkey varies according to region but in general it is 2.0%. Çanakkale is a city in the Aegean region of Turkey but no study about β-thal frequency in Çanakkale has been published to date. In this study, we aimed to investigate the frequency of β-thal mutations in this province. A total of 4452 couples (8904 individuals) applied for premarita...
متن کاملPrevalence of β thalassemia carrier state in Sindhi community of Wardha and evaluation of risk factors for β thalassemia trait.
OBJECTIVE To determine the prevalence of β thalassemia in Sindhi community of Wardha and evaluation of risk factors. To give genetic counseling to those diagnosed as carriers. STUDY DESIGN Cross-sectional (prevalence study). SETTING Sindhi community residing in and around Wardha. STUDY PERIOD 18 months. MATERIALS AND METHODS A total of 578 individuals belonging to Sindhi community resid...
متن کاملPrevalence of −α and ααα alleles in sickle cell trait and β-thalassemia patients in Mexico
The aim of this study was to determine the frequency of α-globin gene mutations in three groups of Mexican unrelated individuals. The first two groups were normal and sickle cell trait individuals from the Costa Chica region, a place with a 12.8% frequency of HbS carriers, and the third group comprised of Mexican mestizo patients with β-thalassemia. We searched for −α and −α α-thalassemia delet...
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ژورنال
عنوان ژورنال: Journal of thee Medical Sciences (Berkala Ilmu Kedokteran)
سال: 2017
ISSN: 0126-1312,2356-3931
DOI: 10.19106/jmedsci004903201702