نتایج جستجو برای: prevention of thalassemia

تعداد نتایج: 21183850  

2014
Manit Nuinoon Kwanta Kruachan Warachaya Sengking Dararat Horpet Ubol Sungyuan

Thalassemia and hemoglobin E (Hb E) are common in Thailand. Individuals with thalassemia trait usually have a normal hemoglobin concentration or mild anemia. Therefore, thalassemic individuals who have minimum acceptable Hb level may be accepted as blood donors. This study was aimed at determining the frequency of α-thalassemia 1 trait, β-thalassemia trait, and Hb E-related syndromes in Souther...

Journal: :acta medica iranica 0
s. ansari p. voosogh s. moshtaghian

life-long red blood transfusion remains the main treatment for severe thalassemia. the development of hemolytic alloantibodies and erythrocyte autoantibodies complicated transfusion therapy in thalassemia patients. the frequency causes and prevention of this phenomenon among 80 transfused thalassemia patients were evaluated in ali asghar children's hospital during 1998-2004 in a cross-sectional...

Journal: :Frontiers in Pediatrics 2023

Thalassemia is an inherited blood disorder imposing a significant social and economic burden. Comprehensive screening strategies are essential for the prevention management of this disease. Third-generation sequencing (TGS), breakthrough technology, has shown great potential diagnostic applications in various diseases, while its application thalassemia detection still infancy. This review aims ...

2011
Sakorn Pornprasert Thanatcha Wiengkum Sarinee Srithep Isarapong Chainoi Panthong Singboottra Sanchai Wongwiwatthananukit

BACKGROUND Prevention and control of thalassemia requires simple, rapid, and accurate screening tests for carrier couples who are at risk of conceiving fetuses with severe thalassemia. METHODS Single-tube multiplex real-time PCR with SYBR Green1 and high-resolution melting (HRM) analysis were used for the identification of α-thalassemia-1 Southeast Asian (SEA) and Thai type deletions and β-th...

ژورنال: پژوهش در پزشکی 2013
اکبری, اکبر, بلوچی, رامین , حیدری مقدم, رشید, قدیمی ایلخانلار, حسن, مرتضوی طباطبائی, سید عبدالرضا,

Abstract Background: Patients with Thalassemia Major suffer from different skeletal deformities. This study was carried out to compare the rate of deformities between patients with Major and minor thalassemia. Materials and Methods: This historical cohort study was done on 87 patients with major thalassemia (case group) and 87 patients with minor thalassemia (control group). Indices of skel...

Journal: :Journal of pediatric hematology/oncology 2007
Hassan Abolghasemi Ali Amid Sirous Zeinali Mohammad H Radfar Peyman Eshghi Mohammad S Rahiminejad Mohammad A Ehsani Hossein Najmabadi Mohammad T Akbari Abdolreza Afrasiabi Haleh Akhavan-Niaki Hamid Hoorfar

PURPOSE To determine the prevalence and geographic distribution of thalassemia and to evaluate the success of the thalassemia prevention and treatment programs in Iran. METHODS Data were obtained from the National Thalassemia Registry of Iran, Iranian Blood Transfusion Organization, genetic laboratories involved in prenatal diagnosis, related pharmaceutical companies, and centers performing b...

A Hashemi, M Noroozi, N Valizadeh, S Hejazi, Sh Nateghi,

Abstract Background Thalassemia patients that are conventionally treated by a regular transfusion regimen are exposed to blood born viral infections.The aim of this study was to investigate the seroprevalence of hepatitis B virus (HBV), hepatitis C virus (HCV) , and human Immunodeficiency virus(HIV) among all multitransfused thalassemia patients in west north of Iran. Material and methods A...

2016
Burçin ŞANLIDAĞ Buse ÇAĞIN Övgü ÖZENLİ Özlem ŞAHALOĞLU Ceyhun DALKAN Nilüfer GALİP Arzu BABAYİĞİT HOCAOĞLU Nerin BAHÇECİLER

BACKGROUND Iron Deficiency Anemia (IDA) is an important health problem all around the world especially in developing countries. In the Mediterranean countries another prevelant reason of anemia is Thalassemia. Certain strategies had been established as a government policy to reduce prevalence in North Cyprus, such as pre-marital screening of Thalassemia. The prevalence of thalassemia trait has ...

دیلمی, آزاده , ولی‌زاده, فرزانه,

Background and purpose: Alpha thalassemia is one of the most common hemoglobin disorders. Some combination of alpha globin gene mutations may cause HbH disease with severe anemia or intermediate thalassemia. In this study we aimed to determine the spectrum of alpha globin gene mutations especially rare mutation at alpha carrier couples in Babolsar, north of Iran. Discovering this spectrum i...

Introduction: Thalassemia can impose adverse effects on the individual, family and community. It is therefore important to specify the needs of children with thalassemia and their parents. This study intended to assess the knowledge and educational needs of adolescents suffering from thalassemia major and active members of the family in Bandar Abbas. Methods: This cross-sectional descriptive...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید