Extended Molecular Spectrum of beta- and alpha-Thalassemia in Oman

Author(s):
Hassan, S.M.; Hamza, N.; Al-Lawatiya, F.J.; Mohammed, A.J.; Harteveld, C.L.; Rajab, A.; Giordano, P.C.
Published
2010
Publication type
Article / Letter to editor

Abstract

Sickle cell disease is known to be very common in the Omani population, although data are limited concerning beta-thalassemia (beta-thal). We report the molecular background of 87 unrelated patients from the Sultanate of Oman, diagnosed with beta-thal major (beta-TM), beta-thal intermedia (beta-TI) or minor. Diagnosis was based on clinical and hematological data and confirmed by molecular analysis. We found 11 different beta-thal determinants in our cohort, which consists of subjects from different regions of Oman. Six of these mutations have not been previously reported in the Omani population. The prevalence of alpha-thal single gene deletions (-alpha

hb-monroe
Date issued
2010-12-31
Language
English
Is part of
Hemoglobin (2010), Vol. 34, no. 2, p. 127-134
hdl
1887/110491
doi
10.3109/03630261003673147