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Primary prevention of hemoglobinopathies by prenatal diagnosis and selective pregnancy termination in a Muslim country: Oman.

Authors :
Hassan, Suha Mustafa
Bakker, Egbert
Harteveld, Cornelis L.
Giordano, Piero C.
Source :
Thalassemia Reports. 2014, Vol. 4 Issue 1, p19-21. 3p.
Publication Year :
2014

Abstract

Hemoglobinopathies (HBP) are the most common genetic disorder in Oman and are in need of prevention programs due to the high incidence of β-thalassemia major and sickle cell disease. Prenatal diagnosis (PD) and selective pregnancy termination is shown to be the most effective prevention tool for the control of HBP. However, PD is not available in Oman thus far because abortion is subject to religious, cultural and ethical issues. We have examined the attitude of a number of Omani HBP carrier couples towards prenatal diagnosis and selective abortion. We have interviewed 35 couples at risk visiting the main premarital clinic in Muscat between Jan 2011 and Jan 2012. Couples were interviewed using a pre-structured questionnaire. The majority would have accepted prenatal diagnosis (94%) if the service would be available in the country but pregnancy termination was greatly influenced by religious values. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20394357
Volume :
4
Issue :
1
Database :
Academic Search Index
Journal :
Thalassemia Reports
Publication Type :
Academic Journal
Accession number :
100044391
Full Text :
https://doi.org/10.4081/thal.2014.4171