نتایج جستجو برای: major ß thalassemia

تعداد نتایج: 639703  

2017
Khadijeh Arjmandi Rafsanjani Maryam Razzaghy-Azar Leila Zahedi-Shoolami Parvaneh Vossough Aliakbar Modarres Nima Taheri

Background: Expansion of bone marrow cavity and decreased cortical and trabecular bone tissues and osteoporosis are resulted from beta-thalassemia. The aim of this study was to assess bone mineral density (BMD) in patients with β thalassemia major and intermedia, and to determine their biochemical and hormonal profiles that may affect BMD. Materials and Methods: In a cross sectional study from ...

2012
Sanjay Gandhi Anita Saxena Archana Gupta

Regular blood transfusion along with iron chelation therapy is a supportive treatment for thalassemia major. Chelation therapy too has its side effects. The most common adverse effects associated with administration of deferiprone are agranulocytosis, neutropenia and arthralgia, primarily, of the large joints. Objective : The study was undertaken to examine the effect of deferiprone on the larg...

2014
Azizollah Arbabisarjou Tahmineh Karimzaei Abdolghaffar Jamalzaei

BACKGROUND Thalassemia Major Disease is not only assumed as a health disorder, but also a social- economic problem in many countries. The costs of transport and preparation of drugs is considered as the greatest problems for more than 63.8% of the patients' families. This study was conducted by aiming at describing biological experience among parents of patients with Thalassemia Major. METHOD...

Extramedullary hematopoiesis (EMH) is a physiological compensatory phenomenon occurring in many hemolytic anemias including thalassemia. Besides transfusion, radiotherapy, surgery or a combination of these modalities, hydroxyurea (HU) as an optimal treatment has been described occasionally. We described a case of beta-thalassemia major who has been on regular blood transfusion and developed EMH...

2016
Antonella Meloni Maria Rita Gamberini Maria Giovanna Neri Maria Chiara Resta Gianluca Valeri Emanuele Grassedonio Cristina Salvatori Monica Benni Antonella Quarta Vincenzo Positano Alessia Pepe

Methods Among the 956 women with hemoglobinopathies in reproductive age enrolled in the Myocardial Iron Overload in Thalassemia (MIOT) project, we selected 17 women with thalassemia (14 with thalassemia major and 3 with transfusion-dependent thalassemia intermedia) who had a pregnancy with successful delivery and who performed a MRI scan before and after the pregnancy. Myocardial and liver iron...

2012
M. Mesbah Uddin Sharif Akteruzzaman Taibur Rahman A. K. M. Mahbub Hasan Hossain Uddin Shekhar

Thalassemia and other structural haemoglobinopathies are the major erythrocyte formation disorder prevalent in certain parts of the world including Bangladesh. We investigated 600 cases of anaemic patients referred from various parts of the country for diagnosis and counselling during 3 months (April to June 2011) of time. The most common form of haemoglobin (Hb) formation disorder observed in ...

2016
George Petrakos Panagiotis Andriopoulos Maria Tsironi

Advances in treatment of thalassemia have led to the aging of thalassemic patients, and consequently concern about successful reproductive outcome is augmented. Although women with thalassemia intermedia only were considered competent of achieving pregnancy, case series reveal the willingness of both thalassemia major and thalassemia intermedia women to have a family. Pregnancy in general is ch...

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