Department of Pediatrics, Dokkyo Medical University, Shimotsuga, Tochigi, Japan.
Cell Biochem Biophys. 2012 Jan;62(1):13-7. doi: 10.1007/s12013-011-9285-2.
Spectral karyotyping is a novel technique for chromosome analysis that has been developed based on the approach of the fluorescence in situ hybridization technique. Spectral karyotyping makes it feasible to diagnose a variety of diseases, because of its technology in painting each of the 24 human chromosomes with different colors. In recent years, it has become possible to adopt the usage of spectral karyotyping for research in general clinical practice, and its usability has attracted particular attention in the diagnosis of different diseases. In this review, we will explain the principle of the spectral karyotyping, as well as its specificity and limitation in detecting the genetic defects within clinical application by presenting two case reports.
光谱核型分析是一种基于荧光原位杂交技术的新型染色体分析技术。光谱核型分析通过为 24 个人类染色体中的每一个都涂上不同的颜色,使其能够诊断多种疾病,这一技术成为可能。近年来,光谱核型分析已在一般临床实践中得到应用,其可用性在不同疾病的诊断中引起了特别关注。在这篇综述中,我们将通过两个病例报告来解释光谱核型分析的原理,以及其在临床应用中检测遗传缺陷的特异性和局限性。