一个俄罗斯常染色体显性非综合征听力损失大家庭中 CEACAM16 基因新型缺义变异的听觉表型

Tatiana G Markova, Natalia N Alekseeva, Oxana P Ryzhkova, Olga L Shatokhina, Anna A Orlova, Viktoriia V Zabnenkova, Olga S Groznova, Olesya V Sagaydak, Svetlana S Chibisova, Alexander V Polyakov, George A Tavartkiladze
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引用次数: 0

摘要

常染色体显性听力损失由大量基因决定。与显性非综合征听力障碍相关的基因已超过 50 个。CEACAM16 基因的致病变体会导致 DFNA4B 型听力损失。目前,该基因中的 8 个致病变体已被描述。本研究的目的是研究一个 CEACAM16 相关常染色体显性非综合征听力损失大家庭的听力学和分子遗传学特征。研究人员收集了详细的病史资料,并对 21 名家庭成员进行了全面的听力检查。进行了基因检测,包括对病例儿子的全基因组测序,以及对病例和所有家庭成员的 Sanger 序列分析。在一个包括五代人的俄罗斯大家庭中,发现了一种常染色体显性遗传的缓慢进展型非综合征晚发听力损失。11 名家庭成员从 5 至 20 岁开始出现听力障碍,最初表现为耳鸣和高频阈值增高。每个人的听力损失都随着年龄的增长而缓慢加重,与老年性听力损失相似。我们在 CEACAM16 基因的第 3 外显子中发现了一个新的可能致病的变异体 с.419С>T (p.(Thr140Ile)) ,该变异体在该家族中与晚发性非综合征性听力损失分离。该家族的临床数据与之前描述的病例的表型相符。总之,这项研究拓宽了该基因的突变范围,有助于开展医学遗传咨询,并回答有关后代听力障碍预后的问题。
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Auditory Phenotype of a Novel Missense Variant in the CEACAM16 Gene in a Large Russian Family With Autosomal Dominant Nonsyndromic Hearing Loss.

Autosomal dominant hearing loss is represented by a large number of genetically determined forms. Over 50 genes associated with dominant nonsyndromic hearing impairments were described. Pathogenic variants in the CEACAM16 gene lead to the development of DFNA4B hearing loss. Currently, 8 pathogenic variants in this gene have been described. The objective of this study was to study the audiological and molecular genetic characteristics of a large family with CEACAM16-associated autosomal dominant nonsyndromic hearing loss. A detailed anamnesis was collected, and a comprehensive audiological examination was performed for 21 family members. Genetic testing was performed, including whole-genome sequencing for the proband's son and Sanger sequence analysis for the proband and for all available family members. In a large Russian family, including 5 generations, an autosomal dominant type of slowly progressing nonsyndromic late-onset hearing loss was observed. Eleven family members suffer from hearing impairment, which starts with tinnitus and threshold increase at high frequencies, since the age of 5-20 years. Hearing loss slowly progresses with age in each person and is similar to age-related hearing loss. We have detected the novel likely pathogenic variant с.419С>T (p.(Thr140Ile)) in exon 3 of the CEACAM16 gene, which segregates with late-onset nonsyndromic hearing loss in this family. The clinical data obtained in the examined family correspond with the phenotype in previously described cases. In general, the study widened the mutation spectrum of the gene, allowing to carry out medical genetic counseling and to answer the questions about the hearing impairment prognosis for future generations.

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