منابع مشابه
Bone marrow transplantation in adult thalassemic patients.
One hundred seven adult patients with thalassemia aged from 17 through 35 years and transplanted from HLA-identical siblings between November 1988 and September 1996 were evaluated on December 31, 1997. The outcome experience of 20 consecutive patients transplanted between November 13, 1988 and January 10, 1991 and reported in September 1992 is updated after 5 additional years. The experience o...
متن کاملHFE gene mutations in Brazilian thalassemic patients.
Hereditary hemochromatosis is a disorder of iron metabolism characterized by increased iron intake and progressive storage and is related to mutations in the HFE gene. Interactions between thalassemia and hemochromatosis may further increase iron overload. The ethnic background of the Brazilian population is heterogeneous and studies analyzing the simultaneous presence of HFE and thalassemia-re...
متن کاملZinc Concentration in Thalassemic Patients Hair
ABSTRACT Thalassemia is a common genetic diseaes. Due to repeated blood transfuion and increasing iron load, deferoxamin is used in this illness. One of it's adverse effect is binding to zinc element, Regarding to effects of zinc on growth and development, when the patient's zinc hair was less than healthy person, it is concluded that with administration of zinc element, There was significant ...
متن کاملDesferioximine induced Ototoxicity in Thalassemic patients
BACKGROUND Thalassemia is a hereditary disorder requiring regular blood transfusion. PURPOSE To determine hearing sensitivity in transfusion-dependent thalassemics who were receiving desferioximine and on oral iron chelation (desferioximine) therapy. METHODS 26 patients with B-thelassemia in the age range of 5-22 years were enrolled in the thalassemia transfusion unit in the Advanced Pediat...
متن کاملEvaluation of salivary immunoglobulin A level in thalassemic patients with periodontitis in comparison with thalassemic patients with healthy periodontium
BACKGROUND AND AIM: This study was conducted to evaluate salivary immunoglobulin A (IgA) level in thalassemic patients with periodontitis in comparison to thalassemic patients with healthy periodontium.METHODS: Seventy-five patients were included in this study and were divided into three groups, group A: 25 major thalassemic patients with mild to moderate periodontitis, group B: 25 thalassemic ...
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ژورنال
عنوان ژورنال: The Professional Medical Journal
سال: 2019
ISSN: 2071-7733,1024-8919
DOI: 10.29309/tpmj/2019.26.02.3079