Literature DB >> 15947927

Hb SE disease: a clinico-hematological profile.

Pravas Mishra1, H P Pati, Tathagat Chatterjee, Ashish Dixit, Dharma R Choudhary, M Upendra Srinivas, Manoranjan Mahapatra, V P Choudhry.   

Abstract

Hb S and Hb E are globally common hemoglobinopathies. However, Hb SE double heterozygous state is uncommon, with only 25 cases reported so far in literature. We present two more cases. One presented with gallstones, and the other was asymptomatic. This type of disorder was previously described as a relatively asymptomatic condition compared to HbSS. A review of the 25 reported cases in literature shows that 40.7% (11/27) of these cases are symptomatic. Gender, hematological parameters and levels of Hb S, E or F do not predict clinical severity.

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Year:  2005        PMID: 15947927     DOI: 10.1007/s00277-005-1044-2

Source DB:  PubMed          Journal:  Ann Hematol        ISSN: 0939-5555            Impact factor:   3.673


  3 in total

Review 1.  HbE/β-Thalassemia and Oxidative Stress: The Key to Pathophysiological Mechanisms and Novel Therapeutics.

Authors:  Rhoda Elison Hirsch; Nathawut Sibmooh; Suthat Fucharoen; Joel M Friedman
Journal:  Antioxid Redox Signal       Date:  2016-11-28       Impact factor: 8.401

Review 2.  Manifestations of HbSE sickle cell disease: a systematic review.

Authors:  Ibrahim Khamees; Fateen Ata; Hassan Choudry; Ashraf T Soliman; Vincenzo De Sanctis; Mohamed A Yassin
Journal:  J Transl Med       Date:  2021-06-16       Impact factor: 5.531

3.  Compound heterozygosity for hemoglobin S and hemoglobin E in a family of Proto-Australoid origin: a case report.

Authors:  Noymi Basumatary; Dipankar Baruah; Paresh Kumar Sarma; Jatin Sarmah
Journal:  J Med Case Rep       Date:  2021-08-02
  3 in total

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