نتایج جستجو برای: beta thalassemia minor

تعداد نتایج: 273056  

Journal: :the journal of tehran university heart center 0
noormohammad noori children and adolescent health research center, aliebne abitaleb hospital, zahedan university of medical sciences, zahedan, iran. mehdi mohamadi children and adolescent health research center, aliebne abitaleb hospital, zahedan university of medical sciences, zahedan, iran. kambiz keshavarz imam sajad hospital, yasuj university of medical sciences, yasuj, iran. seyedmostafa alavi rajaei cardiovascular, medical and research center, tehran university of medical sciences, tehran, iran. maziar mahjoubifard children and adolescent health research center, aliebne abitaleb hospital, zahedan university of medical sciences, zahedan, iran. yalda mirmesdagh rajaei cardiovascular, medical and research center, tehran university of medical sciences, tehran, iran.

background: heart disease is the main cause of mortality and morbidity in patients with beta thalassemia, rendering its early diagnosis vital. we studied and compared echocardiographic findings in patients with beta thalassemia major, patients with beta thalassemia intermedia, and a control group. methods: eighty asymptomatic patients with thalassemia major and 22 asymptomatic cases with thalas...

2011
Sedigheh Amooee Alamtaj Samsami Jamileh Jahanbakhsh Mehran Karimi

BACKGROUND β-thalassemia is the most common hereditary disease in Iran and more than 2 million carriers of the β-thalassemia mutant gene are living in this country. OBJECTIVE To determine pregnancy outcome of women with β-thalassemia minor. MATERIALS AND METHODS In this retrospective, case-control study in two universities affiliated hospitals in Shiraz, all pregnancies occurred between 200...

افتخار, ابراهیم, زارعی پور, مراد علی, شایان مهر, محرم, صدقیانی فر, علی, عباسی, معصومه,

Background and Objective: Beta thalassemia is one of the most prevalent genetic disorders in Iran. Nowadays the premarital screening program for beta thalassemia has brought the highest concern and attention in our country to prevent any child birth affected by the major thalassemia.Thalassemia major leads to serious medical, social, and economic problems for patients and their families, and pa...

ژورنال: Medical Laboratory Journal 2013
Alijanpor, s, Ayatollahi, AA, Joshaghani, HR, Khorasaninejad, R, Roshandel, GH, Royani, s, Shirbaghaei, z,

Abstract Background and Objective: Of the most common hypochromic microcytic anemia are iron deficiency anemia and minor thalassemia, which are common in Iran and their differential diagnosis is extremely important. The level of 25-hydroxy vitamin D is the indication of vitamin D blood status. The aim of this study was to compare serum levels of vitamin D in people with minor thalassemi...

Journal: :international journal of hematology-oncology and stem cell research 0
amir ali hamidieh pediatric hematology- oncology and stem cell transplantation department, hematology- oncology and stem cell transplantation research center, shariati hospital, tehran university of medical sciences, tehran, iran b moradbeag faculty of medicine, qom islamic azad university, qom, iran f pasha faculty of medicine, tehran islamic azad university, tehran, iran mehdi jalili pediatric hematology- oncology and stem cell transplantation department, ematology- oncology and stem cell transplantation research center, shariati hospital, tehran university of medical sciences, tehran, iran m hadjibabaie clinical pharmacology department, faculty of pharmacy, tehran university of medical sciences, tehran, iran m keshavarznia faculty of medicine, qom islamic azad university, qom, iran

introduction: hypoparathyroidism (hpt) is an irreversible but preventable disorder caused by an iron overload which can be considered a typical complication in patients with beta-thalassemia major. patients and method: parathyroid function was evaluated in 130 patients in qom, iran, who suffered from beta-thalassemia major. their serum ferritin levels were checked for monitoring of chelation th...

Journal: :iranian journal of pediatric hematology and oncology 0
a hashemi department of pediatrics, hematology, oncology and genetics research center, shahid sadoughi university of medical scien z hashemian department of pediatrics, hematology, oncology and genetics research center, shahid sadoughi university of medical scienسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید صدوقی یزد (shahid sadooghi university of medical sciences) m ordooei pediatric endocrinologist and professor assistant of pediatric department of shahid sadoughi university of medical scien m amanat medical student, shahid sadoughi university of medical sciences and health services, yazd, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید صدوقی یزد (shahid sadooghi university of medical sciences) f purshamsi medical student, shahid sadoughi university of medical sciences and health services, yazd, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید صدوقی یزد (shahid sadooghi university of medical sciences) n ghasemi department of medical genetic, faculty of medicine, reproductive sciences institute, shahid sadoughi university of medicسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید صدوقی یزد (shahid sadooghi university of medical sciences)

abstract background the aim of the present study was to determine the endocrine dysfunction in patients with major thalassemia, who receive hyper transfusion. materials and methods this cross sectional study was performed during one year, which included 65 major thalassemia patients (31 females and 34 males), aged between 14 month to 27 years old (median 10,3). growth assessment was measured by...

Journal: :iranian red crescent medical journal 0
maryam khavari department of biology, faculty of sciences, zabol university of medical sciences, zabol, ir iran azin hamidi hematology research center, shiraz university of medical sciences, shiraz, ir iran sezaneh haghpanah hematology research center, shiraz university of medical sciences, shiraz, ir iran mohammad hadi bagheri medical imaging research center, shiraz university of medical sciences, shiraz, ir iran marzieh bardestani department of library and information sciences, college of humanities, khouzestan science and research branch, islamic azad university, ahvaz, ir iran razieh hantooshzadeh ministry of health and medical education, tehran, ir iran

background recent studies regarding the effect of hydroxyurea (hu) in thalassemia have revealed favorable effects on the reduction of ineffective erythropoiesis. objectives the aim of the current study was to evaluate whether or not hu can have an effect on the gallstone formation rate in patients with beta-thalassemia intermedia (bti). patients and methods in this case control cross-sectional ...

Journal: :journal of research in medical sciences 0
sezaneh haghpanah hematology research center, shiraz university of medical sciences, shiraz, iran maryam davani hematology research center, shiraz university of medical sciences, shiraz, iran behrang samadi hematology research center, shiraz university of medical sciences, shiraz, iran afsaneh ashrafi a hematology research center, shiraz university of medical sciences, shiraz, iran. mehran karimi prof. of pediatric hematology ,hematology research center

background: beta-thalassemia is considered to be the most frequent hereditary blood disorder worldwide. lipid abnormalities have been detected in different types of beta-thalassemia . the aim of this study is to assess the lipid profiles in beta-thalassemia major (btm) and beta-thalassemia intermedia (bti) patients in southern iran. methods: the study group consisted of 55 btm patients and 50 b...

ژورنال: بیهوشی و درد 2015

Aim and Background: Beta thalassemia major is a hematologic autosomal recessive syndrome. Many anesthetic problems were noted in these patients like difficult intubation, coagulopathies and cardiomyopathies. In this case report, we describe a patient with Beta thalassemia major and intra cranial lipoma. Case report: A 36 year old woman, known case of Beta thalassemia major, was candidate for el...

Journal: :Hereditas 1990
H W Moreira P C Naoum

Haptoglobin types were determined in 626 individuals living in the State of São Paulo (Brazil). Of these, 484 had Hb AA, 31 major beta thalassemia, 43 minor beta thalassemia, 14 Hb SS, and 54 Hb AS. Frequency distribution of the three most common types observed among patients with type beta thalassemia differed significantly from that observed in the Caucasian group with Hb AA. There was a sign...

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