Blood Res.  2016 Sep;51(3):213-214. 10.5045/br.2016.51.3.213.

Delta beta thalassemia: a rare hemoglobin variant

Affiliations
  • 1Department of Haematology, Aga Khan University Hospital, Karachi, Pakistan. huma.omair1986@gmail.com

Abstract

No abstract available.


MeSH Terms

beta-Thalassemia*

Figure

  • Fig. 1 (A) Peripheral blood smear of the patient with anisopoikilocytosis and target cells. (B) Highperformance liquid chromatography showing 100% HbF indicated by the arrow. (C) Pan-cellular pattern on the Kleihauer-Bekte test.


Reference

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3. Khunger JM, Gupta M, Singh R, Kapoor R, Pandey HR. Haematological characterisation and molecular basis of asian Indian inversion deletions delta Beta thalassemia: a case report. J Clin Diagn Res. 2014; 8:FD01–FD02.
Article
4. Verma S, Bhargava M, Mittal S, Gupta R. Homozygous delta-beta thalassemia in a child: a rare cause of elevated fetal hemoglobin. Iran J Ped Hematol Oncol. 2013; 3:222–227. PMID: 24575268.
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6. Silvestroni E, Bianco I, Reitano G. Three cases of homozygous beta, delta-thalassemia (or microcythaemia) with high haemoglobin F in a Sicilian family. Acta Haematol. 1968; 40:220–229. PMID: 4974500.
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