نتایج جستجو برای: beta thalassemia majorcardiac abnormalitiestei index

تعداد نتایج: 584288  

Journal: :Journal of Ayub Medical College, Abbottabad : JAMC 2013
Tazeen Majeed Mohammed Adil Akhter Ujala Nayyar Muhammad Safwan Riaz Jovaria Mannan

BACKGROUND Thalassemia major is one of the most common genetic disorders in Pakistan and over five thousand new patients are added in the pool annually. This familial disease has both medical and social implications, and therefore there is a need to assess the magnitude of beta-Thalassemia trait amongst family members of Thalassemia major patients. METHODS This cross-sectional descriptive stu...

Journal: :international journal of hematology-oncology and stem cell research 0
md. fazlul karim department of biochemistry and molecular biology, university of dhaka, dhaka-1000, bangladesh md ismail department of biochemistry and molecular biology, university of dhaka, dhaka-1000, bangladesh akm mahbub hasan department of biochemistry and molecular biology, university of dhaka, dhaka-1000, bangladesh hossain uddin shekhar department of biochemistry and molecular biology, university of dhaka, dhaka-1000, bangladesh

background: thalassemia is one of the most common hereditary disorders and beta-thalassemia major is its severe form. the present study is concerned with the analysis of liver function, thyroid function and estimation of critical serum ions as well as hematological characteristics in beta-thalassemia patients and controls. subjects and methods: the study included 54 patients with beta-thalassem...

2015
Abdolreza Sotoodeh Jahromi Karamatollah Rahmanian

PURPOSE Patients with beta thalassemia major are at increased risk for bacterial infections specially splenectomized patients. The aim of this study was to determine the anti-tetanus antibody concentration among patients with beta thalassemia major. MATERIALS AND METHODS The anti-tetanus antibody concentration was investigated in 224 patients with thalassemia major and 224 healthy subjects ma...

Journal: :Collegium antropologicum 2009
Asena C Dogramaci Nazan Savas Mehmet A Bagriacik

Dermatoglyphs are cutaneous ridges on the fingers, palms, and soles, formed during early intrauterine life. During this period, and only then, genetic and environmental factors can influence their formation. Beta-thalassemia major is an genetic disease. The aim of the present work was to analyze dermatoglyphs traits in subjects with beta-thalassemia major and their thalassemia carrier parents. ...

Background: The role of phosphate hemostasis in development of thalassemia bone disease has not been extensively studied yet. Due to the lack of sufficient human studies about the changes of serum Fibroblast growth factor-23(FGF23) in patients with beta-thalassemia major as the first step of investigating the role of FGF23 in thalassemia bone disease, the present study aimed to investigate the ...

2012
Indranil Chakrabarti Swapan Kumar Sinha Nilanjana Ghosh Bidyut Krishna Goswami

Background and Objectives: Beta-thalassemia continues to be a cause of significant burden to the society particularly in the poorer developing countries. Although sophisticated methods of screening have become available, a hunt for a cheap, rapid, objective screening method still remains elusive. Thus, the objectives are to study the validity of Naked-Eye-Single-Tube-OsmoticFragility-Test (NEST...

Journal: :Archives of medical research 2008
Mehran Karimi Majid Yavarian Abdolreza Afrasiabi Javad Dehbozorgian Eliezer Rachmilewitz

BACKGROUND beta-thalassemia is the most common inherited single gene disorder worldwide, and glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzyme deficiency. The goal of this study was to compare the frequency of beta-thalassemia trait and G6PD among the Moslem and Jewish populations in Shiraz, southern Iran. METHODS We examined 201 Moslems and 187 Jewish subjec...

Journal: :Archives of hematology case reports and reviews 2021

Beta thalassemia (β thalassemia) is a group of inherited blood disorders. Case report A 17-year old boy accompanied by medical support staff visited our Department for preventive and pediatric dentistry within the University Dental Center Ss.Pantelejmon in Skopje, due to dental pain which comes from first molar tooth(36) low jaw left side.

Background: Atherosclerosis is an important cardiovascular disorder in beta-thalassemia major patients. The present study aimed to predict factors of atherosclerosis in children with beta-thalassemia major. Materials and Methods: This cross-sectional study was conducted on 36 patients with beta-thalassemia major and 36 healthy children as the control group. The carotid intima-media thickness ...

Journal: :Indian pediatrics 1997
S Agarwal R Gulati K Singh

OBJECTIVE To evaluate the molecular make up of hemoglobin E-Beta thalassemia to facilitate diagnosis, genetic counseling and prenatal diagnosis in Uttar Pradesh. DESIGN DNA analysis. SETTING Referred hemolytic anemia cases to Genetics OPD of a tertiary care center. SUBJECTS 21 families of HbE-thalassemia of which 19 were of UP origin. METHODS The patient and obligate carriers in their f...

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