Donoghue Sarah, Downie Lilian, Stutterd Chloe
Aust Fam Physician. 2017;46(4):200-205.
Advances in genomic technology and our understanding of Mendelian disease-causing genes have led to an increased use of genomic testing in clinical practice.
The aim of this paper is to outline recent advances in genetic and genomic testing and the implications for clinical practice.
Next-generation genomic sequencing is improving the diagnostic yield for patients with suspected genetic disease. A molecular diagnosis for a patient with genetic disease can provide information regarding a patient's prognosis, management and reproductive risk, and identify molecular targets for treatment. However, genomic testing frequently identifies variants of uncertain significance. This is illustrated by two case examples.
基因组技术的进步以及我们对孟德尔致病基因的理解,已导致基因组检测在临床实践中的使用增加。
本文旨在概述遗传和基因组检测的最新进展及其对临床实践的影响。
新一代基因组测序正在提高疑似遗传疾病患者的诊断率。对遗传疾病患者的分子诊断可以提供有关患者预后、管理和生殖风险的信息,并确定治疗的分子靶点。然而,基因组检测经常会发现意义不明确的变异。通过两个病例实例对此进行了说明。