Evidence map›Paper›PMID 40998904›Full record

ArticleScientific reports2025

Diagnostic yield of whole exome sequencing with targeted gene analysis in prelingual sensorineural hearing loss in Thailand.

Tasyakorn Damrongchietanon, Duangrurdee Wattanasirichaigoon, Arthaporn Khongkraparn, Saisuda Noojarern, Rattinan Tiravanitchakul, Nittaya Kasemkosin, Sivaporn Kiatthanabumrung, Thipwimol Tim-Aroon, Parith Wongkittichote

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In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Novel splice-site variants inFrontiers in genetics · 2026
    Article
4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Tasyakorn DamrongchietanonDivision of Medical Genetics, Department of Pediatrics, Mahidol University, Bangkok, Thailand.
Duangrurdee WattanasirichaigoonDivision of Medical Genetics, Department of Pediatrics, Mahidol University, Bangkok, Thailand. duangrurdee.wat@mahidol.ac.th.
Arthaporn KhongkraparnDivision of Medical Genetics, Department of Pediatrics, Mahidol University, Bangkok, Thailand.
Saisuda NoojarernDivision of Medical Genetics, Department of Pediatrics, Mahidol University, Bangkok, Thailand.
Rattinan TiravanitchakulDepartment of Communication Sciences and Disorders, Mahidol University, Bangkok, Thailand.
Nittaya KasemkosinDepartment of Communication Sciences and Disorders, Mahidol University, Bangkok, Thailand.
Sivaporn KiatthanabumrungDepartment of Otolaryngology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Thipwimol Tim-AroonDivision of Medical Genetics, Department of Pediatrics, Mahidol University, Bangkok, Thailand.
Parith WongkittichoteDivision of Medical Genetics, Department of Pediatrics, Mahidol University, Bangkok, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prelingual sensorineural hearing loss (SNHL) represents about 80% of genetic SNHL, with at least 90 causative genes identified. In order to identify the genetic diagnosis of prelingual SNHL, we performed a prospective study by systematic history-taking and phenotyping, followed by whole-exome sequencing (WES) with target gene analysis in 100 Thai patients. We found an overall diagnostic yield of 46%, 58.3% for familial cases, and 39.0% for sporadic cases. These included 41 cases with nonsyndromic SNHL(nsSNHL) and 5 cases with syndromic SNHL (sSNHL). We identified 41 P/LP and 4 VUS variants of 15 genes. Of those sSNHL, the causative genes were PAX3, SOX10, MITF (Waardenburg and Teitz syndromes), and SLC26A4 (Pendred syndrome). The genetic defects identified among those with nsSNHL were GJB2 and SLC26A4 as the most prevalent causes, followed by MYO15A, MYO7A, POU3F4, OTOF, PCDH15, GSDME, PTEN, ACTG1, TMPRSS3, MITF, and MPZL2. The inheritance of these nsSNHL genes involved X-linked recessive (n = 3), autosomal dominant (n = 3), and autosomal recessive in the remainder (n = 36). Patients with positive mutations underwent surveillance for associated symptoms like goiter and retinitis pigmentosa. In conclusion, most prelingual SNHL was nsSNHL with autosomal recessive inheritance. Identifying the causative gene benefits patients for specific management and genetic counseling.

Indexed as

Exome SequencingHearing Loss, SensorineuralAdolescentAdultChildChild, PreschoolConnexin 26FemaleGenetic TestingHumansInfantMaleMutationProspective StudiesSulfate TransportersThailandConnexin 26GJB2 protein, humanSLC26A4 protein, humanSulfate TransportersCongenital hearing lossGenetic hearing lossNon-syndromic hearing lossPrelingual hearing lossSensorineural hearing lossWhole exome sequencing

Identifiers

PMID40998904
PMCPMC12464309

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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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 Socratic graph.