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Diagnostic approach to children with birth defects.

作者信息

Pai G S, Gadewar S B

机构信息

Department of Pediatrics, Medical University of South Carolina, Charleston, SC, USA.

出版信息

Indian J Pediatr. 2000 Nov;67(11):819-23. doi: 10.1007/BF02726226.

DOI:10.1007/BF02726226
PMID:11216382
Abstract

Clinical genetics deals with the diagnosis, management and prevention of genetically determined disorders. Our current understanding of the role genes play in the pathogenesis of everything from fetal malformation to neurodegenerative and malignant disorders of late adulthood make it somewhat difficult to draw a clear boundary for this rapidly expanding specialty. With the recent completion of a preliminary draft of the entire sequence of the human genome it is not unreasonable to dream of novel therapeutic approaches such as "gene therapy", to cure disorders heretofore treatable with supportive measures only. Nevertheless, the clinical assessment of the patient will continue to be the cornerstone of good practice of medicine. In this article we review a clinical approach to the diagnostic challenge presented by children with birth defects. The principles we illustrate apply to other aspects of "genetic medicine" as well.

摘要

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本文引用的文献

1
Errors of morphogenesis: concepts and terms. Recommendations of an international working group.形态发生错误:概念与术语。一个国际工作组的建议
J Pediatr. 1982 Jan;100(1):160-5. doi: 10.1016/s0022-3476(82)80261-8.
2
The amniotic band disruption complex: timing of amniotic rupture and variable spectra of consequent defects.羊膜带破裂综合征:羊膜破裂时间及由此产生的各种缺陷谱。
J Pediatr. 1979 Oct;95(4):544-9. doi: 10.1016/s0022-3476(79)80759-3.