Institute for Genomic Statistics and Bioinformatics, Bonn, Germany.
Institute of Human Genetics, School of Medicine, University Hospital Bonn, University of Bonn, Bonn, Germany.
Hum Mutat. 2022 Nov;43(11):1659-1665. doi: 10.1002/humu.24467. Epub 2022 Oct 2.
Next-generation phenotyping (NGP) is an application of advanced methods of computer vision on medical imaging data such as portrait photos of individuals with rare disorders. NGP on portraits results in gestalt scores that can be used for the selection of appropriate genetic tests, and for the interpretation of the molecular data. Here, we report on an exceptional case of a young girl that was presented at the age of 8 and 15 and enrolled in NGP diagnostics on the latter occasion. The girl had clinical features associated with Koolen-de Vries syndrome (KdVS) and a suggestive facial gestalt. However, chromosomal microarray (CMA), Sanger sequencing, multiplex ligation-dependent probe analysis (MLPA), and trio exome sequencing remained inconclusive. Based on the highly indicative gestalt score for KdVS, the decision was made to perform genome sequencing to also evaluate noncoding variants. This analysis revealed a 4.7 kb de novo deletion partially affecting intron 6 and exon 7 of the KANSL1 gene. This is the smallest reported structural variant to date for this phenotype. The case illustrates how NGP can be integrated into the iterative diagnostic process of test selection and interpretation of sequencing results.
下一代表型分析(NGP)是计算机视觉高级方法在医学成像数据中的应用,例如罕见疾病个体的人像照片。对人像进行 NGP 可得出整体评分,用于选择合适的基因检测,并对分子数据进行解读。在此,我们报告了一个特殊病例,一名年轻女孩分别在 8 岁和 15 岁时就诊,并在后者就诊时进行了 NGP 诊断。该女孩具有与 Koolen-de Vries 综合征(KdVS)相关的临床特征和暗示性的面部整体特征。然而,染色体微阵列(CMA)、桑格测序、多重连接依赖性探针分析(MLPA)和 trio 外显子组测序结果仍不确定。鉴于高度提示性的 KdVS 整体评分,决定进行基因组测序以评估非编码变异。该分析显示一个 4.7 kb 的新生缺失部分影响 KANSL1 基因的内含子 6 和外显子 7。这是迄今为止该表型报道的最小结构变异。该病例说明了如何将 NGP 整合到测试选择和测序结果解释的迭代诊断过程中。