Antony Dinu, Nampoory Narayanan, Bacchelli Chiara, Melhem Motasem, Wu Kaman, James Chela T, Beales Philip L, Hubank Mike, Thomas Daisy, Mashankar Anant, Behbehani Kazem, Schmidts Miriam, Alsmadi Osama
Genetics and Genomics Unit, Dasman Diabetes Institute, P.O.Box 1180, Dasman 15462, Kuwait; Genome Research, Human Genetics Department, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences (RIMLS), Geert Grooteplein Zuid 10, 6525GA Nijmegen, The Netherlands.
Dasman Diabetes Institute, P.O.Box 1180, Dasman 15462, Kuwait.
Eur J Med Genet. 2017 Dec;60(12):658-666. doi: 10.1016/j.ejmg.2017.08.019. Epub 2017 Sep 12.
Exome sequencing is becoming widely popular and affordable, making it one of the most desirable methods for the identification of rare genetic variants for clinical diagnosis. Here, we report the clinical application of whole exome sequencing for the ultimate diagnosis of a ciliary chondrodysplasia case presented with an initial clinical diagnosis of Asphyxiating Thoracic Dystrophy (ATD, Jeune Syndrome). We have identified a novel homozygous missense mutation in WDR35 (c.206G > A), a gene previously associated with Sensenbrenner Syndrome, Ellis-van Creveld syndrome and Short-rib polydactyly syndrome type V. The genetic findings in this family led to the re-evaluation of the initial diagnosis and a differential diagnosis of Sensenbrenner Syndrome was made after cautious re-examination of the patient. Cell culture studies revealed normal subcellular localization of the mutant WDR35 protein in comparison to wildtype protein, pointing towards impaired protein-protein interaction and/or altered cell signaling pathways as a consequence of the mutated allele. This research study highlights the importance of including pathogenic variant identification in the diagnosis pipeline of ciliary chondrodysplasias, especially for clinically not fully defined phenotypes.
外显子组测序正变得广泛普及且价格亲民,使其成为临床诊断中鉴定罕见基因变异最理想的方法之一。在此,我们报告了全外显子组测序在一例最初临床诊断为窒息性胸廓发育不良(ATD,Jeune综合征)的纤毛软骨发育异常病例最终诊断中的临床应用。我们在WDR35基因中鉴定出一个新的纯合错义突变(c.206G>A),该基因先前与森氏综合征、埃利斯-范克里维尔德综合征和V型短肋多指综合征相关。该家族的基因发现导致对初始诊断进行重新评估,并在对患者进行谨慎复查后做出了森氏综合征的鉴别诊断。细胞培养研究显示,与野生型蛋白相比,突变型WDR35蛋白的亚细胞定位正常,这表明突变等位基因导致蛋白质-蛋白质相互作用受损和/或细胞信号通路改变。这项研究强调了在纤毛软骨发育异常的诊断流程中纳入致病变异鉴定的重要性,特别是对于临床特征未完全明确的表型。