Molecular diagnosis, clinical evaluation and phenotypic spectrum of Townes-Brocks syndrome: insights from a large Chinese hearing loss cohort

• Published in: Journal of medical genetics Vol. 61; no. 5; pp. 459 - 468
• Main Authors: Yan, Xiaohong, Wang, Jing, Yang, Wen, Li, Linke, Shen, Tian, Geng, Jia, Zhang, Qian, Zhong, Mingjun, Xiong, Wenyu, Bu, Fengxiao, Lu, Yu, Zhao, Yu, Cheng, Jing, Yuan, Huijun
• Format: Journal Article
• Language: English
• Published: England BMJ Publishing Group Ltd 01.05.2024
• Subjects: Abnormalities, Multiple; Adaptor Proteins, Signal Transducing - genetics; Anus, Imperforate; Diagnostics; Genetic Carrier Screening; Genetic Diseases, Inborn; Hearing Loss, Sensorineural - diagnosis; Hearing Loss, Sensorineural - genetics; Humans; Mutation; Nuclear Proteins - genetics; Otolaryngology; Phenotype; Syndrome; Thumb - abnormalities; Transcription Factors - genetics; Otolaryngology; Genetic Diseases, Inborn; Genetic Carrier Screening
• ISSN: 0022-2593; 1468-6244
• DOI: 10.1136/jmg-2023-109579

BackgroundTownes-Brocks syndrome (TBS) is a rare genetic disorder characterised by multiple malformations. Due to its phenotypic heterogeneity and rarity, diagnosis and recognition of TBS can be challenging and there has been a lack of investigation of patients with atypical TBS in large cohorts and delineation of their phenotypic characteristics.MethodsWe screened SALL1 and DACT1 variants using next-generation sequencing in the China Deafness Genetics Consortium (CDGC) cohort enrolling 20 666 unrelated hearing loss (HL) cases. Comprehensive clinical evaluations were conducted on seven members from a three-generation TBS family. Combining data from previously reported cases, we also provided a landscape of phenotypes and genotypes of patients with TBS.ResultsWe identified five novel and two reported pathogenic/likely pathogenic (P/LP) SALL1 variants from seven families. Audiological features in patients differed in severity and binaural asymmetry. Moreover, previously undocumented malformations in the middle and inner ear were detected in one patient. By comprehensive clinical evaluations, we further provide evidence for the causal relationship between SALL1 variation and certain endocrine abnormalities. Penetrance analysis within familial contexts revealed incomplete penetrance among first-generation patients with TBS and a higher disease burden among their affected offspring.ConclusionThis study presents the first insight of genetic screening for patients with TBS in a large HL cohort. We broadened the phenotypic-genotypic spectrum of TBS and our results supported an underestimated prevalence of TBS. Due to the rarity and phenotypic heterogeneity of rare diseases, broader spectrum molecular tests, especially whole genome sequencing, can improve the situation of underdiagnosis and provide effective recommendations for clinical management.