Literature DB >> 9178316

Acceptance of first-trimester prenatal diagnosis for the haemoglobinopathies in Lebanon.

L Zahed1, J Bou-Dames.   

Abstract

We have interviewed 83 couples at risk for a haemoglobin disorder, mostly beta-thalassaemia, in an effort to evaluate their attitude towards first-trimester prenatal diagnosis. Most of the families had received poor education and were of low socio-economic status and more than half of the couples were not properly aware of their genetic risk. Fifty-nine per cent of the couples were definitely in favour of prenatal diagnosis, 23 per cent were uncertain at the time of the interview, and 18 per cent were opposed to such testing, because of their religious conviction against termination of a pregnancy. Another important factor which seems to influence choice was the cost of the test. Essential issues that arise from this study include the importance of a control programme adapted to particular populations, proper information and counselling, and the need for financial support in countries such as Lebanon.

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Year:  1997        PMID: 9178316     DOI: 10.1002/(sici)1097-0223(199705)17:5<423::aid-pd68>3.0.co;2-p

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  15 in total

1.  Molecular basis of oculocutaneous albinism type 1 in Lebanese patients.

Authors:  Laila Zahed; Hala Zahreddine; Baha' Noureddine; Nelly Rebeiz; Nadine Shakar; Pierre Zalloua; Fadi Haddad
Journal:  J Hum Genet       Date:  2005-06-04       Impact factor: 3.172

2.  Assessing Parental Knowledge About Thalassemia in a Thalassemia Center of Karachi, Pakistan.

Authors:  Humaira Maheen; Farrukh Malik; Barera Siddique; Asim Qidwai
Journal:  J Genet Couns       Date:  2015-04-07       Impact factor: 2.537

3.  Attitudes and beliefs among high- and low-risk population groups towards β-thalassemia prevention: a cross-sectional descriptive study from India.

Authors:  Swati Chawla; Rajnish Kumar Singh; Bhaskar V K S Lakkakula; Raghavendra Rao Vadlamudi
Journal:  J Community Genet       Date:  2017-04-06

4.  Epidemiological profile of common haemoglobinopathies in Arab countries.

Authors:  Hanan A Hamamy; Nasir A S Al-Allawi
Journal:  J Community Genet       Date:  2012-12-08

5.  A holistic approach to education programs in thalassemia for a multi-ethnic population: consideration of perspectives, attitudes, and perceived needs.

Authors:  Li Ping Wong; Elizabeth George; Jin-Ai Mary Anne Tan
Journal:  J Community Genet       Date:  2011-02-24

6.  Attitudes towards prenatal diagnosis and abortion in a multi-ethnic country: a survey among parents of children with thalassaemia major in Malaysia.

Authors:  Chin Fang Ngim; Nai Ming Lai; Hishamshah Ibrahim; Vanassa Ratnasingam
Journal:  J Community Genet       Date:  2013-01-08

7.  Decisions about testing and termination of pregnancy for different fetal conditions: a qualitative study of European White and Pakistani mothers of affected children.

Authors:  Shenaz Ahmed; Jenny Hewison; Josephine M Green; Howard S Cuckle; Janet Hirst; Jim G Thornton
Journal:  J Genet Couns       Date:  2008-10-09       Impact factor: 2.537

8.  Decisions Regarding Pregnancy Termination Due to β-Thalassemia Major: a Mixed-Methods Study in Sistan and Baluchestan, Iran.

Authors:  Zahra Moudi; Ebrahim Miri-Moghaddam
Journal:  J Genet Couns       Date:  2016-09-28       Impact factor: 2.537

9.  Ethical, social, and cultural issues related to clinical genetic testing and counseling in low- and middle-income countries: a systematic review.

Authors:  Adrina Zhong; Benedict Darren; Bethina Loiseau; Li Qun Betty He; Trillium Chang; Jessica Hill; Helen Dimaras
Journal:  Genet Med       Date:  2018-08-03       Impact factor: 8.822

10.  Preimplantation genetic diagnosis in Saudi Arabia.

Authors:  Zeinab Abotalib
Journal:  Bioinformation       Date:  2013-04-30
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