Literature DB >> 5470095

Ascertainment and prevention of genetic disease.

A E Emery, C Smith.   

Abstract

A genetic register system has been developed for the ascertainment and prevention of genetic disease. Its potential value is illustrated with data collected from 478 families with serious genetic disorders which had been seen during the past five years. Of these 249 were referred specifically for genetic counselling, autosomal dominant disorders accounting for the largest group of families with individuals at high risk of becoming affected. Of 717 individuals at high risk of having affected children (or carrier daughters in the case of X-linked recessive disorders), only 101 were referred specifically for counselling. Many were referred only after the birth of an affected child which might otherwise have been prevented. A genetic register system linked to practitioner, hospital, and health department records could be a valuable means of preventing genetic disease.

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Year:  1970        PMID: 5470095      PMCID: PMC1701725          DOI: 10.1136/bmj.3.5723.636

Source DB:  PubMed          Journal:  Br Med J        ISSN: 0007-1447


  5 in total

1.  The rationale of genetic counseling.

Authors:  E A Murphy
Journal:  J Pediatr       Date:  1968-01       Impact factor: 4.406

2.  The combined use of a central registry and vital records for incidence studies of congenital defects.

Authors:  D H Renwick
Journal:  Br J Prev Soc Med       Date:  1968-04

3.  Genetic counselling in lethal X-linked disorders.

Authors:  A E Emery; R Morton
Journal:  Acta Genet Stat Med       Date:  1968

4.  Genetics of common disorders.

Authors:  C O Carter
Journal:  Br Med Bull       Date:  1969-01       Impact factor: 4.291

5.  Family-oriented follow-up.

Authors:  V A McKusick
Journal:  J Chronic Dis       Date:  1969-06
  5 in total
  7 in total

1.  A report on genetic registers. Based on the report of the Clinical Genetics Society Working Party.

Authors:  A E Emery; C Brough; M Crawfurd; P Harper; R Harris; G Oakshott
Journal:  J Med Genet       Date:  1978-12       Impact factor: 6.318

2.  Genetic registers.

Authors:  M E Pembrey
Journal:  Arch Dis Child       Date:  1979-03       Impact factor: 3.791

3.  A genetic register system (RAPID).

Authors:  A E Emery; D Elliott; M Moores; C Smith
Journal:  J Med Genet       Date:  1974-06       Impact factor: 6.318

4.  PKU screening.

Authors:  H C Soltan
Journal:  Can Med Assoc J       Date:  1973-04-21       Impact factor: 8.262

5.  Individuals at risk in families with genetic disease.

Authors:  C Smith; S Holloway; A E Emery
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318

6.  Wishes of patients with retinitis pigmentosa concerning genetic counselling.

Authors:  S Bundey; S J Crews
Journal:  J Med Genet       Date:  1982-08       Impact factor: 6.318

7.  Attitudes of patients and their relatives to Huntington's disease.

Authors:  R Stern; R Eldridge
Journal:  J Med Genet       Date:  1975-09       Impact factor: 6.318

  7 in total

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