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A Chinese Male with Normal Hematological Indices and High Hb A2 Levels in β-Thalassemia Trait.

Yi-Jun ChenYou-Qiong LiQing LiuLan-Yan TangFu-Tong Lv
Published in: Hemoglobin (2020)
β-Thalassemia (β-thal) is a common hematological disorder in the Guangxi Zhuang Autonomous Region of Southern China. Heterozygous β-thal is usually associated with reduced hematological indices and increased Hb A2 levels. However, the preventive program of the regional government only conducts the screening of hematological indices [complete blood count (CBC)] especially at primary hospitals. In this study, we describe a male β-thal patient presenting normal hematological indices but with a high Hb A2 level. We proposed that hemoglobin (Hb) analysis and CBC should be performed together in the preventive screening program in regions with a high thalassemia incidence to avoid misdiagnosis.
Keyphrases
  • sickle cell disease
  • case report
  • quality improvement
  • risk factors
  • early onset
  • gene expression