贝苏夫大学医院b型地中海贫血重症患者血清硒、锰水平的测定

M. Meabed, Esraa Shafey
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引用次数: 0

摘要

: Β-地中海贫血(Β- tm)是最常见的遗传性单基因疾病之一。地中海贫血儿童通常生长发育不良,青春期发育迟缓。硒和锰是导致地中海贫血患者生长和青春期障碍的因素。贝尼苏夫大学医院儿科血液学门诊地中海贫血患者血清硒和锰水平的评估对50例重型乙型地中海贫血患儿和50例正常患儿进行全病史采集,并以全血细胞计数、血清铁蛋白、血清硒、锰为对照进行全面检查和调查。β-地中海贫血患者血清锰水平高于正常对照组,P值为0.000;血清硒水平与正常对照组相比差异不显著,P值为0.119。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment Of Serum Level Of Selenium And Manganese In B-Thalassemia Major Patients In Beni-Suef University Hospital
: Β- thalassemia major (β-TM) is one of the most common inherited single gene disorder .Children with Thalassemia frequently have poor growth and delayed pubertal development. Selenium and manganese are factors responsible for growth and puberty disorders in thalassemic patients. Assessment of serum levels of selenium and manganese in patients with thalassemia in Pediatric Haematology Clinic in Beni Suef University Hospital. Blood was taken from 50 pediatric patients with b thalassemia major, and 50 normal children as controls all were subjected to full history taking and full examination and investigation was done in the form of CBC, serum Ferritin , serum Selenium and Manganese . Patients with β- thalassemia major have high serum manganese level as compared to normal controls with P value of (0.000), while serum selenium level is insignificant as compared to normal controls with P value of (0.119)
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