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典型和非典型 branchio-oto-renal 综合征患者的表型-基因型相关性。

Phenotype-genotype correlation in patients with typical and atypical branchio-oto-renal syndrome.

机构信息

Department of Otolaryngology, Kyorin University, Tokyo, Japan.

Division of Hearing and Balance Research, National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, 2-5-1 Higashigaoka Meguro-ku, Tokyo, 152-8902, Japan.

出版信息

Sci Rep. 2022 Jan 19;12(1):969. doi: 10.1038/s41598-022-04885-w.

Abstract

Some patients have an atypical form of branchio-oto-renal (BOR) syndrome, which does not satisfy the diagnostic criteria, despite carrying a pathogenic variant (P variant) or a likely pathogenic variant (LP variant) of a causative gene. P/LP variants phenotypic indices have yet to be determined in patients with typical and atypical BOR syndrome. We hypothesized that determining phenotypic and genetic differences between patients with typical and atypical BOR syndrome could inform such indices. Subjects were selected from among patients who underwent genetic testing to identify the cause of hearing loss. Patients were considered atypical when they had two major BOR diagnostic criteria, or two major criteria and one minor criterion; 22 typical and 16 atypical patients from 35 families were included. Genetic analysis of EYA1, SIX1, and SIX5 was conducted by direct sequencing and multiplex ligation-dependent probe amplification. EYA1 P/LP variants were detected in 25% and 86% of atypical and typical patients, respectively. Four EYA1 P/LP variants were novel. Branchial anomaly, inner ear anomaly, and mixed hearing loss were correlated with P/LP variants. Development of refined diagnostic criteria and phenotypic indices for atypical BOR syndrome will assist in effective detection of patients with P/LP variants among those with suspected BOR syndrome.

摘要

一些患者具有非典型的 branchio-oto-renal (BOR) 综合征形式,尽管携带致病变异 (P 变异) 或可能致病的变异 (LP 变异),但不符合诊断标准。在具有典型和非典型 BOR 综合征的患者中,尚未确定 P/LP 变异的表型指数。我们假设确定典型和非典型 BOR 综合征患者之间的表型和遗传差异可以提供这些指数。从接受基因检测以确定听力损失原因的患者中选择受试者。当患者具有两个主要 BOR 诊断标准,或两个主要标准和一个次要标准时,被认为是非典型的;35 个家庭中有 22 个典型和 16 个非典型患者入选。通过直接测序和多重连接依赖性探针扩增对 EYA1、SIX1 和 SIX5 进行基因分析。在非典型和典型患者中分别检测到 25%和 86%的 EYA1 P/LP 变异。发现了四个新的 EYA1 P/LP 变异。鳃裂异常、内耳异常和混合性听力损失与 P/LP 变异相关。制定更精细的非典型 BOR 综合征诊断标准和表型指数将有助于有效检测疑似 BOR 综合征患者中的 P/LP 变异患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/420c/8770796/8e03ebe39b74/41598_2022_4885_Fig1_HTML.jpg

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