نتایج جستجو برای: thalassemia preventing program

تعداد نتایج: 555836  

2013
H Hashemizadeh R Noori

BACKGROUND Beta thalassemia is a preventable disease. Iran has about 20,000Patients who are homozygote for β-thalassaemia and 3,750,000 carriers. The aim of this study was to determine the prevalence of beta thalassemia minor among men who underwent premarital screening in Quchana city in Khorasan Razavi region of Iran. MATERIALS AND METHODS This research is a descriptive cross-sectional stud...

2008
H Hourfar M Heidari M Kheirollahi M Miryounesi

Background: β-thalassemia is a common autosomal recessive disorder resulting from over 200 different mutations of beta globin genes. The aim of the present study was to identify the distribution and frequency of the most common β-thalassemia mutations among the population of Isfahan Province in central Iran. Methods: The data presented here were derived from a total of 114 β-thalassemia chromos...

Journal: :Haematologica 2014
Francesca Rossi Silverio Perrotta Giulia Bellini Livio Luongo Chiara Tortora Dario Siniscalco Matteo Francese Marco Torella Bruno Nobili Vincenzo Di Marzo Sabatino Maione

The pathogenesis of bone resorption in β-thalassemia major is multifactorial and our understanding of the underlying molecular and cellular mechanisms remains incomplete. Considering the emerging importance of the endocannabinoid/endovanilloid system in bone metabolism, it may be instructive to examine a potential role for this system in the development of osteoporosis in patients with β-thalas...

Journal: :Turkish journal of haematology : official journal of Turkish Society of Haematology 2007
Kaan Savaş Gülleroğlu Nazan Sarper Ayşe Sevim Gökalp

In addition to premarital screening programs, education of the general population is important in preventing hemoglobinopathies. The aim of the present study was the education of university students. Short questionnaires were applied before and after a prepared lecture. A 20-minute audiovisual education was provided including the clinical characteristics and inheritance of thalassemia and sickl...

2017
Azam Moosavi Ali M. Ardekani

BACKGROUND β-thalassemia is the most common monogenic disorder in Iran, and one of the challenges in the screening of the carriers is the coinheritance of α-thalassemia mutations. In the view of high prevalence of α-thalassemia mutations in many parts of the country, the aim of this study was to determine the carrier frequency of common alpha deletions, as a secondary modifier in clinical manif...

2016
Zahra Molazem Roghaye Noormohammadi Roya Dokouhaki Maryam Zakerinia Zahra Bagheri

BACKGROUND Excessive iron accumulation in the visceral organs creates problems for patients with beta-thalassemia major. Despite chelation therapy, mortality rate from the complications of this disease is still quite high. OBJECTIVES This study aimed to investigate the effectiveness of nutrition, exercise, and a praying program at reducing iron overload in patients with beta-thalassemia major...

H Hashemizadeh , R Noori ,

Abstract Background Beta thalassemia is a preventable disease. Iran has about 20,000Patients who are homozygote for β-thalassaemia and 3,750,000 carriers. The aim of this study was to determine the prevalence of beta thalassemia minor among men who underwent premarital screening in Quchana city in Khorasan Razavi region of Iran Materials and Methods This research is a descriptive cross-sect...

Journal: :Jurnal obsesi : jurnal pendidikan anak usia dini 2023

Prevalensi penyakit thalassemia di Jawa Barat mengalami peningkatan setiap tahunnya. Program pencegahan sekunder thalasemia yaitu pada keluarga yang beresiko atau dicurigai sebagai pembawa sifat untuk mencegah terjadi kembali kelahiran dengan mayor. Tujuan penelitian ini mengidentifikasi hubungan antara kesadaran orang tua anak penderita prilaku thalasemia. Desain adalah cross-sectional study s...

2018
Yeşim Aydınok Yeşim Oymak Berna Atabay Gönül Aydoğan Akif Yeşilipek Selma Ünal Yurdanur Kılınç Banu Oflaz Mehmet Akın Canan Vergin Melike Sezgin Evim Ümran Çalışkan Şule Ünal Ali Bay Elif Kazancı Talia İleri Didem Atay Türkan Patıroğlu Selda Kahraman Murat Söker Mediha Akcan Aydan Akdeniz Mustafa Büyükavcı Güçhan Alanoğlu Özcan Bör Nur Soyer Nihal Özdemir Karadaş Ezgi Uysalol Meral Türker Arzu Akçay Süheyla Ocak Adalet Meral Güneş Hüseyin Tokgöz Elif Ünal Naci Tiftik Zeynep Karakaş

OBJECTIVE The Turkish Society of Pediatric Hematology set up a National Hemoglobinopathy Registry to demonstrate the demographic and disease characteristics of patients and assess the efficacy of a hemoglobinopathy control program (HCP) over 10 years in Turkey. MATERIALS AND METHODS A total of 2046 patients from 27 thalassemia centers were registered, of which 1988 were eligible for analysis....

Journal: :Indian pediatrics 2007
Mehran Karimi Alireza Fotouhi Ghiam Alireza Hashemi Saied Alinejad Mahmood Soweid Sara Kashef

OBJECTIVE This study was conducted to assess bone mineral density (BMD) and bone mineral content (BMC) in patients with thalassemia major and intermedia, and to correlate them with biochemical and hematological profile. DESIGN 106 thalassemic patients (49 major and 57 intermedia) were scanned by dual energy xray absorptiometry technique for BMD and BMC at lumbar spine and femoral neck. The ef...

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