نتایج جستجو برای: thalassemia intermedia

تعداد نتایج: 23663  

Journal: :Cold Spring Harbor Perspectives in Medicine 2012

Emamdadi A, Fadaie M, Naderi M, Nouri NM, Rajaie S,

Background: Cardiac dysfunction due to chronic anemia and hemosiderosis are the major causes of death among patients with thalassemia intermedia. This study was performed to compare the cardiac function in thalassemia intermedia patients with normal subjects by means of echocardiography. Materials and Methods: This was a case-control study performed on 22 patients affected by thalassemia int...

2011
Catherine Badens Philippe Joly Imane Agouti Isabelle Thuret Katia Gonnet Synda Fattoum Alain Francina Marie-Claude Simeoni Anderson Loundou Serge Pissard

A cohort of 106 patients included in the French National Registry for Thalassemia were genotyped for 5 genetic modifiers of severity: (i) beta-thalassemia mutations, (ii) the XmnI SNP, (iii) the -3.7 kb alpha-thal deletion, (iv) the tag-SNP rs 11886868 in BCL11A exon 2 and (v) the tag-SNP rs9399137 in the HBSB1L-cMYB inter-region. Multivariate analysis was performed to study the risk of Thalass...

2017
Alexandra Agapidou Paul King Cecilia Ng Dimitris A. Tsitsikas

Beta thalassemia dominant results from mutations in the β globin chain gene resulting in the production of elongated, highly unstable beta globin chains. Several such mutations have been described and in a heterozygous state they may confer a phenotype more severe than that of β thalassemia trait and lead to a clinical syndrome of thalassemia intermedia and its associated complications such as ...

Journal: :Journal of clinical and diagnostic research : JCDR 2014
Jitender Mohan Khunger Monika Gupta Rekha Singh Rohit Kapoor Hare Ram Pandey

The hereditary persistence of fetal hemoglobin (HPFH) and delta beta thalassemia are heterogeneous disorders characterised by increased levels of fetal hemoglobin and high level of this Hb continues in adulthood. The distinction between these two conditions is not always possible with routine hematologic analysis and molecular characterisation of the defect is required. We encountered such a ra...

Journal: :The Journal of Tepecik Education and Research Hospital 2003

Journal: :Lebanese Medical Journal 2014

Journal: :Indian Journal of Hematology and Blood Transfusion 2013

Journal: :international journal of hematology-oncology and stem cell research 0
fereshteh maryami biotechnology research center, department of molecular medicine, pasteur institute of iran, tehran, iran azita azarkeivan pediatric hematology oncology, transfusion research center, high institute for research and education in transfusion medicine, department of thalassemia clinic, tehran, iran mohammad sadegh fallah kawsar human genetics research center, tehran, iran sirous zeinali iranian molecular medicine network, biotechnology research center, pasteur institute of iran, pasteur st, tehran, iran kawsar human genetics research center, tehran, iran

background: thalassemia syndromes are the most prevalent single gene disorders in iran. this study aimed to evaluate the effect of different types of beta-globin gene mutations, co-inheritance of alpha-globin gene mutations and/or xmn1 snp on disease phenotype in a large cohort of iranian patients. subjects and methods: in total, 433 patients were clinically classified into β-thalassemia major ...

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