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检测胎儿异常。

Detecting fetal abnormalities.

作者信息

Williamson R

机构信息

Murdoch Institute for Research into Birth Defects, University of Melbourne.

出版信息

Aust Fam Physician. 1997 Mar;26(3):245-9, 252-3.

PMID:9078657
Abstract

Three per cent of infants suffer from birth defects, (mostly genetic) including single gene diseases, such as cystic fibrosis or thalassaemia; chromosomal aneuploidies such as Down syndrome; or multifactorial conditions such as spina bifida and congenital heart defects. Perhaps the most important reason for focusing attention on genetics in 1997 is that the field has changed dramatically due to advances in technology and in our understanding of the human genome. New opportunities for prevention combined with more effective treatment, represent the new standard of care that the community has the right to expect for genetic disease. This article looks at antenatal diagnosis early in pregnancy and reviews what progress is to be expected in this field during the coming decade.

摘要

3%的婴儿患有出生缺陷(大多为遗传性),包括单基因疾病,如囊性纤维化或地中海贫血;染色体非整倍体疾病,如唐氏综合征;或多因素疾病,如脊柱裂和先天性心脏缺陷。1997年将关注重点放在遗传学上的最重要原因或许是,由于技术进步以及我们对人类基因组认识的深入,该领域已发生了巨大变化。预防方面的新机遇与更有效的治疗相结合,代表了社会有权期望的遗传疾病新护理标准。本文探讨了孕期早期的产前诊断,并回顾了未来十年该领域有望取得的进展。

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