Molecular Identification of a Rare Haemoglobin Variant: Hb G Coushatta in Malaysia
Keywords:
Haemoglobin variant, Hb G Coushatta, molecular analysis.Abstract
Thalassaemia screening programme was conducted to reduce the burden of the disease [1]. Here, we describe one unexpected discovery in a 33-year-old gentleman and also the importance of DNA analysis in detecting the globin gene mutation.Â
Case report:
A male patient was screened for haemoglobin (Hb) variant after his wife was noted to have beta thalassaemia trait during her antenatal checkup. Otherwise, he was asymptomatic. He had a normal Hb (16.09 g/L), an increased red blood cell (RBC) count (5.91x10^6/μL) with a borderline mean corpuscular volume (80.7 fL) and a borderline mean corpuscular haemoglobin (27.1 pg). The RBCs on peripheral blood smear, appeared hypochromic microcytic. A prominent band was seen at the S region on alkaline Haemoglobin electrophoresis (Fig. 1), which was not showed in the high performance liquid chromatography. Instead, there was a significant increase in Hb A2/E (42.7%), a great reduction in Hb A (45.6%) and normal Hb F value (0.3%).Â
In capillary electrophoresis, an abnormal peak was observed in Hb D zone (40.8%) with normal Hb A2 (2.6%) The screening methods would indicate Hb E, Hb D or Hb S. But none of these were shown by at least two of the methods. Therefore, beta-globin gene sequencing was carried out, which revealed Hb G Coushatta mutation [β22(B4)(GAA→GCA)] (Fig. 2).
Hb analysis may be useful in quantifying the Hb variant. However, definitive diagnosis by molecular analysis is required for identifying the rare mutation such as Hb G Coushatta. Although the variant carries no significance in clinical manifestations [2], it is still important to identify the rare mutation as it can be passed on to the next generation and may evolve to different haplotypes.
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References
Ezalia, et. al., Thalassaemia Screening among Healthy Blood Donors in Hospital Tengku Ampuan Rahimah, Klang. Med & Health, 2014. 9(1): p. 44-52.
Steinberg, M. H., et. al., Disorders of Haemoglobin: Genetics, Pathophysiology, and Clinical Management. Cambridge University Press, 2009. p. 600-601.
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