Rational use of genetic tests in internal medicine. Possibilities and limitations of next generation sequencing diagnostics

被引:1
|
作者
Elbracht, M. [1 ]
Meyer, R. [1 ]
Eggermann, T. [1 ]
Kurth, I. [1 ]
机构
[1] Uniklin RWTH Aachen, Inst Humangenet, Pauwelsstr 30, D-52074 Aachen, Germany
来源
INTERNIST | 2018年 / 59卷 / 08期
关键词
Genetic counselling; Sequence analysis; DNA; Genome; Exome; Gene panel analysis; MEDICAL GENETICS; AMERICAN-COLLEGE; GUIDELINES; VARIANTS; GENOMICS;
D O I
10.1007/s00108-018-0457-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
New methods of molecular genetic diagnostics enable a more comprehensive genetic analysis of patients. Rational use and benefits of molecular genetic testing in patients with various internal diseases. Evaluation of topic-related literature, discussion of own experiences, as well as consideration of current guidelines. New genetic tests, such as next generation sequencing (NGS), improve the diagnosis of hereditary diseases; however, the use of this technology also leads to additional findings, which must be carefully considered. The rational use of genetic tests is a benefit for patients and can significantly influence the prevention and treatment of a disease. The increasing complexity of genetic findings requires interdisciplinary approaches involving human genetics, internal medicine, and other disciplines.
引用
收藏
页码:756 / 765
页数:10
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