Report of Beta Thalassemia in Newar Ethinicity
作者: Rajendra Dev Bhatt
作者单位: 1Kathmandu University-School of Medical Sciences, Dhulikhel Hospital-Kathmandu university Hospital
刊名: Annals of Clinical Chemistry and Laboratory Medicine, 2018, Vol.3 (1), pp.30-34
来源数据库: Annals of Clinical Chemistry and Laboratory Medicine
DOI: 10.3126/acclm.v3i1.17298
原始语种摘要: Beta thalassemia trait is a heterogeneous autosomal recessive form of beta thalassemia. Individual with beta thalassemia are clinically asymptomatic. Here we have described a case that has been incidentally diagnosed as beta thalassemia trait. A 31 year old male form Newar Community came to hospital for routine health checkup was send for hematological investigation. On examination, his red cell morphology was found to be microcytic hypochromic and his hemoglobin concentration was mildly decrease. His other parameters was evaluated and requested for analysis of iron profile and hemoglobin electrophoresis. Iron profile test was normal. Hemoglobin electrophoresis showed prominent band in HbA2 region. Presence of HbA2 band was confirmed by hemoglobin variant HPLC analysis. A diagnosis of...
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  • thalassemia 地中海贫血
  • hemoglobin 血红蛋白
  • Beta β
  • asymptomatic 无症状的
  • hypochromic 减色的
  • microcytic 小红细胞
  • mildly 缓和地
  • hematological 血液学的
  • profile 纵断图
  • trait 性状