Diagnostic Outcome of Genetic Testing for Neuromuscular Disorders in a Tertiary Center.

Q3 Medicine
Husam Al Sultani, Komal Hafeez, Aziz Shaibani
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引用次数: 0

Abstract

Abstract: Genetic testing is an effective and reliable modality in clinical neuromuscular diagnosis. The recent developments in testing methods and increasing reliance on genetic testing in clinical practice require more studies to examine the benefits and advantages of such tests. We examined the results of single-gene sequencing/repeat analysis, panels, and whole-genome sequencing (WES) of 514 tests of 393 patients. All patients were suspected of a neuromuscular disorder and the samples were either WBC or muscle tissue. 28.60% (n.147) of the tests were positive while 23.74% (n.122) were VUS. In single-gene sequencing/repeat analysis, 43.08% were positive, in panels, 23.17% were positive, while 30.00% were positive in WES. Our results showed consistency with current studies and improvement of the utility of genetic testing. Although some obstacles are identified, providing statistical data can support more usage and popularity of genetic testing among physicians and patients.

三级中心神经肌肉疾病基因检测的诊断结果。
摘要基因检测是临床神经肌肉诊断中一种有效、可靠的方法。测试方法的最新发展和临床实践中对基因测试的日益依赖需要更多的研究来检查这种测试的好处和优势。我们检查了393例患者的514项测试的单基因测序/重复分析、面板和全基因组测序(WES)的结果。所有患者都被怀疑患有神经肌肉疾病,样本要么是白细胞,要么是肌肉组织。阳性检出率为28.60% (n.147),阴性检出率为23.74% (n.122)。单基因测序/重复分析阳性率为43.08%,面板阳性率为23.17%,WES阳性率为30.00%。我们的研究结果与目前的研究结果一致,并表明基因检测的实用性有所提高。尽管存在一些障碍,但提供统计数据可以支持医生和患者更多地使用和普及基因检测。
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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
64
期刊介绍: Journal of Clinical Neuromuscular Disease provides original articles of interest to physicians who treat patients with neuromuscular diseases, including disorders of the motor neuron, peripheral nerves, neuromuscular junction, muscle, and autonomic nervous system. Each issue highlights the most advanced and successful approaches to diagnosis, functional assessment, surgical intervention, pharmacologic treatment, rehabilitation, and more.
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