Evidence map›Paper›PMID 39161163›Full record

ArticleThe journal of international advanced otology2024

Investigation of Targeted Genes and Identification of Novel Variants with Next Generation Sequencing Method in Hearing Loss.

Drenushe Zhuri, Hazal Sezginer Guler, Sinem Yalcintepe, Selma Demir, Engin Atli, Emine Ikbal Atli, Hakan Gurkan

Abstract read
In one paragraph

Article in The journal of international advanced otology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Drenushe ZhuriDepartment of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Türkiye.
Hazal Sezginer GulerDepartment of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Türkiye.
Sinem YalcintepeDepartment of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Türkiye.
Selma DemirDepartment of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Türkiye.
Engin AtliDepartment of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Türkiye.
Emine Ikbal AtliDepartment of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Türkiye.
Hakan GurkanDepartment of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hearing loss is a widespread condition throughout the world. It may affect patients from newborns to the elderly. There are too many reasons for hearing loss, including congenital hearing loss, virus infections, age-related situations, and traumatic situations, which may be related to the immune-mediated system. Fifty percent of hearing loss is related to genetic mutations and defects; genetic causes are highly heterogeneous, so the analysis of new variants are important for diagnosis. We aimed to describe the importance of detected gene variations by using targeted gene panels in the Next-Generation-Sequencing (NGS) platform. Eighty-one hearing loss targeted genes were investigated using Illumina NextSeq550 technology in 100 participants with hearing loss between 2017 and 2022 in our Genetic Diseases Evaluation Center. Targeted genes were performed on 100 patients with hearing loss diagnosis. The total number of detected variants was 77. Forty-seven cases have likely pathogenic/pathogenic variants. Thirty of them have uncertain clinical significance variants, and from the detected variants, 8 are novel. In this research, we highlighted that earlier detection of hearing loss using molecular genetic methods may help us understand the etiology and orient for a better prognosis. Results detected by using the NGS platform can assist and improve the diagnosis. In this study, the diagnostic rate with targeted genes was detected as 35.29%. It has an important role in clinical practice as the recommendation of cochlear implants. Clarifying the genotype and phenotype correlation helps us figure out the etiology of hearing loss and also the worth of genetic counseling in hereditary hearing loss.

Indexed as

Hearing LossHigh-Throughput Nucleotide SequencingAdolescentAdultAgedChildChild, PreschoolFemaleGenetic TestingGenetic VariationHumansInfantInfant, NewbornMaleMiddle AgedMutation

Identifiers

PMID39161163
PMCPMC11363168

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.