Literature DB >> 1670797

Cuban programme for prevention of sickle cell disease.

H Granda1, S Gispert, A Dorticós, M Martín, Y Cuadras, M Calvo, G Martínez, M A Zayas, J A Oliva, L Heredero.   

Abstract

The percentage of carriers of the sickle cell gene in Cuba ranges from 3 to 7% in different regions. In 1983 the National Medical Genetics Centre initiated a programme for the control of sickle cell disease, which was started in Havana and later extended nationwide. The programme is based on mass education, screening and supportive genetic counselling, care of affected individuals, and availability of prenatal diagnosis. 806,935 pregnant women had been screened by the end of 1989: 29,913 (3.7%) were heterozygous, homozygous or doubly heterozygous for abnormal haemoglobin. 19,686 fathers (67%) were also tested: 1268 at-risk couples were detected. 531 elected to have prenatal diagnosis; 404 results were obtained and 98 affected fetuses (SS or SC) found. In 72 cases the pregnancy was terminated.

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Year:  1991        PMID: 1670797     DOI: 10.1016/0140-6736(91)90810-c

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


  6 in total

1.  A national screening policy for sickle cell disease and thalassaemia major for the United Kingdom. Questions are left after two evidence based reports.

Authors:  A Streetly
Journal:  BMJ       Date:  2000-05-20

2.  Prevention of sickle cell disease: observations on females with the sickle cell trait from the Manchester project, Jamaica.

Authors:  Karlene Mason; Felicea Gibson; Ruth-Ann Gardner; Beryl Serjeant; Graham R Serjeant
Journal:  J Community Genet       Date:  2015-12-02

3.  Prenatal screening for hemoglobinopathies.

Authors:  J E Bowman
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025

Review 4.  Prevention and control of haemoglobinopathies.

Authors:  M Angastiniotis; B Modell; P Englezos; V Boulyjenkov
Journal:  Bull World Health Organ       Date:  1995       Impact factor: 9.408

5.  Global epidemiology of haemoglobin disorders and derived service indicators.

Authors:  Bernadette Modell; Matthew Darlison
Journal:  Bull World Health Organ       Date:  2008-06       Impact factor: 9.408

6.  Prenatal genetic counseling for hemoglobinopathy carriers: a comparison of primary providers of prenatal care and professional genetic counselors.

Authors:  P T Rowley; S Loader; C J Sutera; A Kozyra
Journal:  Am J Hum Genet       Date:  1995-03       Impact factor: 11.025

  6 in total

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