Literature DB >> 1532425

UK clinicians' knowledge of and attitudes to the prenatal diagnosis of single gene disorders.

H V Firth1, R H Lindenbaum.   

Abstract

Postal questionnaires were sent to 308 clinicians in the UK (general practitioners, obstetricians, clinical geneticists, neurologists, paediatricians, and paediatric neurologists) to assess their knowledge of, and attitudes to, the prenatal diagnosis of three common single gene disorders, Huntington's disease (HD), cystic fibrosis (CF), and Duchenne muscular dystrophy (DMD). Replies received numbered 213, a response rate of 69%. Overall, 95% of responding clinicians thought that offering prenatal diagnosis for the three test conditions was often or always appropriate. There was a correlation between the clinicians' estimates of life expectancy and their willingness to offer prenatal diagnosis (p less than 0.01). Among the non-geneticists questioned, fewer than 50% of general practitioners answered correctly regarding the availability of prenatal tests.

Entities:  

Keywords:  Empirical Approach; Genetics and Reproduction

Mesh:

Year:  1992        PMID: 1532425      PMCID: PMC1015815          DOI: 10.1136/jmg.29.1.20

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  8 in total

1.  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

2.  Demand for DNA probe testing in three genetic centres in Britain (August 1986 to July 1987).

Authors:  R J Rona; A V Swan; R Beech; L Prentice; A Reynolds; O Wilson; G Mole; P Vadera
Journal:  J Med Genet       Date:  1989-04       Impact factor: 6.318

3.  First-trimester fetal diagnosis for haemoglobinopathies: three cases.

Authors:  J M Old; R H Ward; M Petrou; F Karagözlu; B Modell; D J Weatherall
Journal:  Lancet       Date:  1982-12-25       Impact factor: 79.321

4.  Dystrophin: the protein product of the Duchenne muscular dystrophy locus.

Authors:  E P Hoffman; R H Brown; L M Kunkel
Journal:  Cell       Date:  1987-12-24       Impact factor: 41.582

5.  Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA.

Authors:  J R Riordan; J M Rommens; B Kerem; N Alon; R Rozmahel; Z Grzelczak; J Zielenski; S Lok; N Plavsic; J L Chou
Journal:  Science       Date:  1989-09-08       Impact factor: 47.728

6.  Attitudes of general practitioners to presymptomatic testing for Huntington's disease.

Authors:  M E Mennie; S M Holloway; D J Brock
Journal:  J Med Genet       Date:  1990-04       Impact factor: 6.318

7.  A consortium approach to molecular genetic services. Scottish Molecular Genetics Consortium.

Authors:  D J Brock
Journal:  J Med Genet       Date:  1990-01       Impact factor: 6.318

8.  Prenatal diagnosis for the detection of Down syndrome: why are so few eligible women tested?

Authors:  A Lippman-Hand; M Piper
Journal:  Prenat Diagn       Date:  1981-10       Impact factor: 3.050

  8 in total
  7 in total

1.  Preimplantation genetic diagnosis: does age of onset matter (anymore)?

Authors:  Timothy Krahn
Journal:  Med Health Care Philos       Date:  2008-11-01

2.  Clinical genetics meets primary care.

Authors:  N Qureshi; J A Raeburn
Journal:  BMJ       Date:  1993-10-02

3.  Knowledge of genetics among residents in obstetrics and gynecology.

Authors:  M A Kershner; E A Hammond; A E Donnenfeld
Journal:  Am J Hum Genet       Date:  1993-12       Impact factor: 11.025

4.  Genetic susceptibility to cancer. Family physicians' experience.

Authors:  June C Carroll; Judith Belle Brown; Sean Blaine; Gord Glendon; Patricia Pugh; Wendy Medved
Journal:  Can Fam Physician       Date:  2003-01       Impact factor: 3.275

5.  Expanded carrier screening in reproductive healthcare: perspectives from genetics professionals.

Authors:  D Cho; M L McGowan; J Metcalfe; R R Sharp
Journal:  Hum Reprod       Date:  2013-04-14       Impact factor: 6.918

6.  The knowledge value-chain of genetic counseling for breast cancer: an empirical assessment of prediction and communication processes.

Authors:  Nabil Amara; Jolyane Blouin-Bougie; Jalila Jbilou; Norrin Halilem; Jacques Simard; Réjean Landry
Journal:  Fam Cancer       Date:  2016-01       Impact factor: 2.375

7.  A sociobehavioural perspective on genetic testing and counselling for heritable breast, ovarian and colon cancer.

Authors:  K G Macdonald; B Doan; M Kelner; K M Taylor
Journal:  CMAJ       Date:  1996-02-15       Impact factor: 8.262

  7 in total

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