نتایج جستجو برای: beta thalassemia minor

تعداد نتایج: 273056  

Journal: :iranian journal of blood and cancer 0
karimi m marvasti ve mehrabanejad s mohaghegh p afrasiabi a dehbozorgian j

background: hb a2 is elevated in subjects with beta thalassemia minor but small percent of carriers have normal hb a2 with elevated levels of hbf (2-10%). this type of thalassemia is called delta beta thalassemia, and can be missed in pre-marriage hematologic consults or screening which leads to increased risk of child birth with beta thalassemia major. materials and methods: in this prospectiv...

Journal: :medical journal of islamic republic of iran 0
mahdi shahriari pediatric hematology – oncology department, nemazee hospital, shiraz university of medical sciences, shiraz, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences)سازمان های دیگر: nemazee hospital, sezaneh haghpanah hematology research center, shiraz university of medical sciences, shiraz, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences)سازمان های دیگر: hematology research center javad dehghani hematology research center, shiraz university of medical sciences, shiraz, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences)سازمان های دیگر: hematology research center javad dehbozorgian hematology research center, shiraz university of medical sciences, shiraz, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences)سازمان های دیگر: hematology research center peyman eatemadfar hematology research center, shiraz university of medical sciences, shiraz, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences)سازمان های دیگر: hematology research center asghar bazrafshan hematology research center, shiraz university of medical sciences, shiraz, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences)سازمان های دیگر: hematology research center

background :highserum level of cancer antigen 15.3 (ca15.3) has been reported in some malignant and nonmalignant conditions including thalassemia major which could have been resulted from ineffective erythropoiesis. we aimed to evaluate the serum level of ca15.3 in carriers of beta-thalassemia by comparing them with cancer patients and healthy individuals.   methods : this cross-sectional study...

Background: Until now, no study has been reported investigating the association between β-thalassemia minor and Helicobacter pylori (H. pylori) infection. This study was designed to compare H. pylori infection rate between β-thalassemia minor patients and healthy controls. Methods: A number of 100 β-thalassemia minor patients (50 males, 50 females) and 100 gender-matched healthy...

Afrasiabi A, Bazrafshan A, Dehbozorgian J, Karimi M, Marvasti VE, Mehrabanejad S, Mohaghegh P, Silavizadeh S,

Background: Hb A2 is elevated in subjects with beta thalassemia minor but small percent of carriers have normal Hb A2 with elevated levels of HbF (2-10%). This type of thalassemia is called delta beta thalassemia, and can be missed in pre-marriage hematologic consults or screening which leads to increased risk of child birth with beta thalassemia major. Materials and Methods: In this prospe...

  Background :Highserum level of cancer antigen 15.3 (CA15.3) has been reported in some malignant and nonmalignant conditions including thalassemia major which could have been resulted from ineffective erythropoiesis. We aimed to evaluate the serum level of CA15.3 in carriers of beta-thalassemia by comparing them with cancer patients and healthy individuals.   Methods : This cross-sectional stu...

Journal: :مجله بین المللی علوم آزمایشگاهی 0
kave tari amir atashi farshid karami fatemeh kiani nodeh mohammad shahjahani

background and aims: iron deficiency anemia (ida) and beta thalassemia minor (btm) are the most common hypochromic microcytic anemias, and it is regarded important to differentiate between them. several formulae can be taken into consideration based on red blood cell (rbc) parameters in order to distinguish between these two disorders. hence, the present study intended to evaluate the sensitivi...

Journal: :iranian journal of pathology 2007
foroogh sadat hashemi maryam abolhasani seyed mohammad hakimi

introduction and objective: zinc as the second trace element of the human body plays an important role in numerous functions. a large number of research studies have showed serum zinc deficiency and excess urinary excretion in patients with major beta thalassemia, but few studies revealed excess urinary zinc excretion in minor beta thalassemia and no study investigated serum zinc levels in this...

Foroogh sadat Hashemi, Maryam Abolhasani, Seyed Mohammad Hakimi

Introduction and Objective: Zinc as the second trace element of the human body plays an important role in numerous functions. A large number of research studies have showed serum zinc deficiency and excess urinary excretion in patients with major beta thalassemia, but few studies revealed excess urinary zinc excretion in minor b...

Journal: :Blood 1981
C Q Edwards M H Skolnick J P Kushner

A pedigree was studied in which five individuals with beta-thalassemia minor were found to have nontransfusional hemochromatosis. Three were children under the age of 10 and two were young male adults, ages 28 and 33. A 5-yr-old child without evidence of thalassemia also had hemochromatosis. Since hemochromatosis is transmitted as an HLA-linked autosomal recessive disorder, HLA haplotypes serve...

Journal: :Annals of clinical and laboratory science 1992
J P Crowley J B Metzger E W Merrill C R Valeri

Patients with heterozygous beta-thalassemia minor have a decreased hematocrit (HCT). Since the HCT is a primary determinant of whole blood viscosity, the known reduction in HCT in beta-thalassemia minor should lead to a measurable reduction of whole blood viscosity. The influence of the relatively lower mean corpuscular volume and consequent higher red blood cell count and beta-thalassemia mino...

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