نتایج جستجو برای: hba2
تعداد نتایج: 435 فیلتر نتایج به سال:
Dennis O Mook-Kanamori ([email protected]) Sandra WK de Kort ([email protected]) Cornelia M van Duijn ([email protected]) Andre G Uitterlinden ([email protected]) Albert Hofman ([email protected]) Henriëtte A Moll ([email protected]) Eric AP Steegers ([email protected]) Anita CS Hokken-Koelega ([email protected]) Vincent WV Jaddoe (v.jaddoe@erasmusm...
Using a genome-wide association study, we found that common inter-individual differences in haemoglobin A(2) (HbA(2) , α(2) δ(2) ) levels are largely governed by genetic factors (42% of variability). The influence of age (1%) and sex (4%) was small. HbA(2) levels were influenced by two loci: the HBS1L-MYB locus on chromosome 6q, which has been shown to have pleiotropic effects on other haemat...
Background: Thalassemia syndromes are the commonest genetic disorders of blood and constitute a vast public health problem with 2.78 to 4% prevalence in India. The most effective feasible approach reduce incidence thalassemia major is implementation carrier screening program screen antenatal women early pregnancy. Methods: Institutional based cross sectional observational study was conducted. W...
چکیده مقدمه: کم خونی و فقر آهن و خصیصه بتاتالاسمی از شایع ترین علل کم خونی هیپوکرومیک میکروسیتیک می باشند. جهت افتراق این دو بیماری، فرمول هایی بر پایه اندکس های گلبول قرمز وجود دارد که در این مطالعه به بررسی ارزش این اندکس ها پرداخته می شود. نویسنده مسئول: دکتر مصطفی روان بخش بخش پاتولوژی بیمارستان شهیدمحمدی، دانشگاه علوم پزشکی هرمزگان بندرعباس- ایران تلفن: 9177675403 98+ پست الکترونیکی: mosta...
چکید ه سابقه و هدف هموگلوبینوپاتی شایع ترین اختلال تک ژنی در ایران است. استان سیستان و بلوچستان ، 2300 بیمار هموگلوبینوپاتی وابسته به دریافت خون در جنوب شرق ایران دارد. در این مطالعه فراوانی هموگلوبینوپاتی ها در سطح استان مورد ارزیابی قرار گرفت. مواد و روش ها این مطالعه توصیفی ـ تحلیلی بر روی 2129 نفر در طیف سنی 10- 5 سال که با روش نمونه گیری خوشه ای چند مرحله ای انتخاب شده بودند، انجام...
We describe 27 cases of mild-to-severe α-thalassemia (α-thal) syndrome caused by interaction of Hb Adana [α59(E8)Gly→Asp, GGC>GAC (α2)] with deletional and nondeletional α(+)-thal mutations in Indonesian patients. Hematological profiles and clinical manifestations of all patients were assessed by routine procedures. The genotypes were generated by a multiplex-polymerase chain reaction (m-PCR), ...
ABSTRACT Thalassemia is a genetic disease, which is prevalent in Guilan province. In order to detect thalassemia gene carries, Screening program was performed in high school students of the Rasht City, with cooperation of Guilan Medical University. Complete blood count and blood indices were reviewed in 22136 students, and Hb. Electrophoresis (with helena equipment) were performed in cases wi...
Cyanosis in an apparently healthy newborn baby may be caused by hemoglobin variants associated with the formation of methemoglobin, collectively known as M hemoglobins. They should not be confused with genetic alterations in methemoglobin reductase enzyme systems of red cells since treatment and prognosis are completely different. A newborn male child was noted to be significantly cyanotic at b...
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