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
相关论文
共 50 条
  • [21] Next-generation sequencing meets genetic diagnostics: Development of a comprehensive workflow for neuromuscular disorders
    Kesari, A.
    Punetha, J.
    Uapinyoying, P.
    Clarke, N.
    Waddell, L.
    North, K.
    Plotz, P.
    Tesi-Rocha, C.
    Bonnemann, C.
    Grosmann, C.
    Bertorini, T.
    Hoffman, E.
    NEUROMUSCULAR DISORDERS, 2013, 23 (9-10) : 795 - 795
  • [22] Genetic tests by next-generation sequencing in children with developmental delay and/or intellectual disability
    Han, Ji Yoon
    Lee, In Goo
    CLINICAL AND EXPERIMENTAL PEDIATRICS, 2020, 63 (06) : 195 - 202
  • [23] Defining a pipeline to use next generation sequencing for genetic testing in hereditary cancer
    Lazaro, Conxi
    Lopez-Doriga, Adriana
    Castellsague, Ester
    del Valle, Jesus
    Tornero, Eva
    Moreno, Victor
    Pineda, Marta
    Gonzalez, Sara
    Fellubadalo, Lidia
    Capella, Gabriel
    CANCER RESEARCH, 2012, 72
  • [24] Pediatric Neurologist Use of Next-Generation Sequencing Diagnostics: Current State and Future Prospects
    Helman, G. T.
    Taft, R. J.
    Bonkowsky, J. L.
    Eichler, F. S.
    Pizzino, A.
    Vanderver, A.
    ANNALS OF NEUROLOGY, 2015, 78 : S201 - S201
  • [25] Neurologist Comfort in the Use of Next-Generation Sequencing Diagnostics Current State and Future Prospects
    Helman, Guy
    Bonkowsky, Joshua L.
    Vanderver, Adeline
    JAMA NEUROLOGY, 2016, 73 (06) : 621 - 622
  • [26] Genetic diagnostics of early childhood hearing loss: better testing with Next-Generation DNA Sequencing
    Sommen, M.
    Van Camp, G.
    B-ENT, 2013, 9 : 51 - 56
  • [27] PRECISION MEDICINE FOR PEDIATRIC DIABETES THROUGH A RAPID GENETIC TEST USING NEXT GENERATION SEQUENCING
    Schwitzgebel, V.
    Dirlewanger, M.
    Klee, P.
    Blouin, J. -L.
    SWISS MEDICAL WEEKLY, 2018, 148 : 68S - 68S
  • [28] Personalized and Predictive Medicine for Pediatric Diabetes Through a Genetic Test Using Next Generation Sequencing
    Schwitzgebel, Valerie
    Klee, Philippe
    Dirlewanger, Mirjam
    Blouin, Jean-Louis
    HORMONE RESEARCH IN PAEDIATRICS, 2018, 90 : 83 - 84
  • [29] Use of next-generation DNA sequencing to analyze genetic variants in rheumatic disease
    Graham B Wiley
    Jennifer A Kelly
    Patrick M Gaffney
    Arthritis Research & Therapy, 16
  • [30] Use of next-generation DNA sequencing to analyze genetic variants in rheumatic disease
    Wiley, Graham B.
    Kelly, Jennifer A.
    Gaffney, Patrick M.
    ARTHRITIS RESEARCH & THERAPY, 2014, 16 (06)