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Parental experience of whole genome sequencing for children with sensorineural hearing loss
Otorhinolaryngology, Head and Neck Surgery, Department of Clinical Sciences Lund, Lund University, Lund, Sweden; Department of Otorhinolaryngology, Skåne University Hospital, Lund, Sweden.ORCID iD: 0000-0001-8056-4911
Örebro University, School of Medical Sciences. Örebro University Hospital. Otorhinolaryngology, Head and Neck Surgery, Department of Clinical Sciences Lund, Lund University, Lund, Sweden; Department of Otorhinolaryngology, Örebro University, Örebro, Sweden.
Otorhinolaryngology, Head and Neck Surgery, Department of Clinical Sciences Lund, Lund University, Lund, Sweden; Department of Otorhinolaryngology, Skåne University Hospital, Lund, Sweden.ORCID iD: 0000-0002-2417-5767
Department of Otorhinolaryngology, Skåne University Hospital, Lund, Sweden; Logopedics, Phoniatrics and Audiology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
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2026 (English)In: International Journal of Qualitative Studies on Health and Well-being, ISSN 1748-2623, E-ISSN 1748-2631, Vol. 21, no 1, article id 2641802Article in journal (Refereed) Published
Abstract [en]

Purpose: The purpose of this in-depth interview study was to explore how parents of children with sensorineural hearing loss (SNHL) experienced genetic testing and whether they experienced risks and benefits.

Background: Most children with SNHL have a genetic etiology, which can be identified through genetic sequencing. A genetic test does not influence treatment, and whether patients and parents perceived genetic tests as valuable is unclear.

Methods: In this study, 10 parents of children with SNHL who underwent genetic testing were interviewed, and the content was analyzed using inductive thematic analysis.

Results: Three global themes were identified. In the first theme, (1) Limited knowledge creates uncertainty, parents described uncertainty related to the information provided, the test result itself and child-related factors. The second theme, (2) Genetic knowledge is considered important for the family and the future, explored the importance of knowledge. Parents wanted an explanation to make the future predictable, and the test had practical implications. In the last category, (3) Knowledge adds complexity and can be challenging, ethical considerations and risks associated with knowledge were highlighted.

Conclusion: The main conclusion was that parents experienced that genetic testing provided valuable personal information and had practical implications. However, a genetic diagnosis can cause concern and may affect family planning.

Place, publisher, year, edition, pages
Taylor & Francis, 2026. Vol. 21, no 1, article id 2641802
Keywords [en]
Sensorineural hearing loss, genetic sequencing, parental experiences, thematic analysis, interview study
National Category
Public Health, Global Health and Social Medicine
Research subject
Disability research
Identifiers
URN: urn:nbn:se:oru:diva-127950DOI: 10.1080/17482631.2026.2641802ISI: 001714011300001PubMedID: 41820818OAI: oai:DiVA.org:oru-127950DiVA, id: diva2:2045728
Funder
Hörselskadades Riksförbund, FA22- 0001Available from: 2026-03-13 Created: 2026-03-13 Last updated: 2026-03-20Bibliographically approved

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Värendh, MariaWidén, Stephen

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