Literature DB >> 9175458

Pre-marriage prevention of thalassaemia: report of a 100,000 case experience in Isfahan.

M Ghanei1, P Adibi, M Movahedi, M A Khami, R L Ghasemi, T Azarm, B Zolfaghari, H R Jamshidi, R Sadri.   

Abstract

BACKGROUND: Iran like other middle east countries has a large number of major thalassaemics. Due to religious restrictions on abortion, the routine prevention of the birth of thalassaemic children by this means is not possible. The aim of this study is to describe an alternative means to prevent the birth of thalassaemic children.
METHODS: From January 1993 to January 1996, 10,000 people preparing for marriage were screened for the thalassaemia trait, using CBC and HbA2 level measurement. High risk couples were referred for further consultation regarding the disease and the means of its prevention. The proposed actions of the couples regarding thalassaemia prevention were evaluated immediately after consultation and then re-evaluated three months later. RESULT: After the project had been running for three years the average of high risk couple initially deciding not to marry was 90% and no new cases of thalassemia were detected in the children of the screened population.
CONCLUSION: Where both members of the couple were trait-positive their preferred choice was not to marry, rather than to marry and use other or no methods of preventing a thalassemia affected child being born to them. Cultural and religious ideas can affect such decisions and in some Islamic countries the establishment and use of a genetic counselling centre can help prevent most of new thalassaemia cases.

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Year:  1997        PMID: 9175458     DOI: 10.1016/s0033-3506(97)00574-x

Source DB:  PubMed          Journal:  Public Health        ISSN: 0033-3506            Impact factor:   2.427


  6 in total

1.  Frequency of β-thalassemia trait and other hemoglobinopathies in northern and western India.

Authors:  Nishi Madan; Satendra Sharma; S K Sood; Roshan Colah; Late H M Bhatia
Journal:  Indian J Hum Genet       Date:  2010-01

2.  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

3.  The Reproductive Behavior of Families with Thalassemic Children in Hormozgan.

Authors:  Ali Safari Moradabadi; Azin Alavi; Tasnim Eqbal Eftekhaari; Sakineh Dadipoor
Journal:  J Reprod Infertil       Date:  2015 Jul-Sep

Review 4.  Genetic epidemiology, hematological and clinical features of hemoglobinopathies in Iran.

Authors:  Zohreh Rahimi
Journal:  Biomed Res Int       Date:  2013-06-18       Impact factor: 3.411

5.  Unique pattern of mutations in β-thalassemia patients in Western Uttar Pradesh.

Authors:  Ajay F Christopher; Anita Kumari; Sunali Chaudhary; Sandhya Hora; Ziledar Ali; Satish C Agrawal
Journal:  Indian J Hum Genet       Date:  2013-04

Review 6.  The Iran Thalassemia Prevention Program: Success or Failure?

Authors:  M Hashemieh; H Timori Naghadeh; M Tabrizi Namini; H Neamatzadeh; M Hadipour Dehshal
Journal:  Iran J Ped Hematol Oncol       Date:  2015-07-20
  6 in total

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