Literature DB >> 6150377

Effect of fetal diagnostic testing on birth-rate of thalassaemia major in Britain.

B Modell, M Petrou, R H Ward, D V Fairweather, C Rodeck, L A Varnavides, J M White.   

Abstract

A programme of prospective heterozygote detection and counselling, fetal diagnostic testing, and abortion of fetuses affected by thalassaemia major introduced in Britain in 1977 has proved highly acceptable to at-risk couples of Cypriot and East African Asian origin, but less so to couples of Pakistani origin. However, many at-risk couples are still not detected prospectively, the proportion of thalassaemia-major births prevented was only 32% by the end of 1981, and there is little evidence of a further fall since then. The thalassaemia-major birth-rate had fallen by 60% in Cypriots and by 20% in East African Asians, but it had not fallen at all in Pakistanis. Improved approaches to fetal diagnosis of thalassaemia major are becoming available, so a concerted effort is needed to inform all the at-risk ethnic groups of the existence of the problem and the possibility of detection of affected fetuses.

Mesh:

Year:  1984        PMID: 6150377     DOI: 10.1016/s0140-6736(84)92070-1

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  7 in total

1.  Informed choice in genetic screening for thalassaemia during pregnancy: audit from a national confidential inquiry.

Authors:  B Modell; R Harris; B Lane; M Khan; M Darlison; M Petrou; J Old; M Layton; L Varnavides
Journal:  BMJ       Date:  2000-02-05

2.  Molecular genetics in the National Health Service in Britain.

Authors:  R Harris; R Elles; D Craufurd; A Dodge; A Ivinson; K Hodgkinson; R Mountford; M Schwartz; T Strachan; A Read
Journal:  J Med Genet       Date:  1989-04       Impact factor: 6.318

3.  Principles and practicalities of carrier screening: attitudes of recent parents.

Authors:  J M Green
Journal:  J Med Genet       Date:  1992-05       Impact factor: 6.318

4.  The frequency of consanguineous marriage among British Pakistanis.

Authors:  A Darr; B Modell
Journal:  J Med Genet       Date:  1988-03       Impact factor: 6.318

5.  Prenatal diagnosis of sickle hemoglobinopathies: the experience of the Columbia University Comprehensive Center for Sickle Cell Disease.

Authors:  M C Driscoll; N Lerner; K Anyane-Yeboa; J Maidman; D Warburton; K Schaefer-Rego; R Hsu; C Ince; J Malin; M Pallai
Journal:  Am J Hum Genet       Date:  1987-06       Impact factor: 11.025

6.  Congenital rubella in babies of south Asian women in England and Wales: an excess and its causes.

Authors:  E Miller; A Nicoll; S A Rousseau; P J Sequeira; M H Hambling; R W Smithells; H Holzel
Journal:  Br Med J (Clin Res Ed)       Date:  1987-03-21

7.  Genetic risk: women's understanding of carrier risks in Duchenne muscular dystrophy.

Authors:  E P Parsons; A J Clarke
Journal:  J Med Genet       Date:  1993-07       Impact factor: 6.318

  7 in total

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