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遗传病的诊断与预防。

Ascertainment and prevention of genetic disease.

作者信息

Emery A E, Smith C

出版信息

Br Med J. 1970 Sep 12;3(5723):636-7. doi: 10.1136/bmj.3.5723.636.

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.

摘要

已开发出一种基因登记系统,用于确定和预防遗传疾病。从过去五年中诊治的478个患有严重遗传疾病的家庭收集的数据说明了该系统的潜在价值。其中249个家庭是专门因遗传咨询前来就诊的,常染色体显性疾病占高危个体家庭的最大比例。在717个有生育患病子女高风险的个体中(对于X连锁隐性疾病,则是生育携带致病基因女儿的高风险个体),只有101个是专门因咨询前来就诊的。许多人是在患病子女出生后才前来就诊的,而这些患病子女原本是可以预防的。与从业者、医院和卫生部门记录相连接的基因登记系统可能是预防遗传疾病的一种宝贵手段。

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Ascertainment and prevention of genetic disease.遗传病的诊断与预防。
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引用本文的文献

本文引用的文献

1
Family-oriented follow-up.
J Chronic Dis. 1969 Jun;22(1):1-7. doi: 10.1016/0021-9681(69)90081-2.
2
Genetics of common disorders.常见疾病的遗传学
Br Med Bull. 1969 Jan;25(1):52-7. doi: 10.1093/oxfordjournals.bmb.a070671.
3
Genetic counselling in lethal X-linked disorders.致死性X连锁疾病的遗传咨询
Acta Genet Stat Med. 1968;18(6):534-42. doi: 10.1159/000152177.
5
The rationale of genetic counseling.
J Pediatr. 1968 Jan;72(1):121-30. doi: 10.1016/s0022-3476(68)80415-9.

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