Parental experience of whole genome sequencing for children with sensorineural hearing loss

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.

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Publication Details

Journal
International Journal of Qualitative Studies on Health and Well-Being
Published
2026-03-12
DOI
https://doi.org/10.1080/17482631.2026.2641802
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.00
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article

Parental experience of whole genome sequencing for children with sensorineural hearing loss

Karin Stenfeldt, Johanna Elander, Stephen Widén, Maria Värendh et al.
International Journal of Qualitative Studies on Health and Well-Being
Genomics and Rare Diseases
article

Parental experience of whole genome sequencing for children with sensorineural hearing loss

Karin Stenfeldt, Johanna Elander, Stephen Widén, Maria Värendh, Johannes K. Ehinger
article en

Abstract

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.

International Journal of Qualitative Studies on Health and Well-BeingVol. 21(1)
Lund University (SE), Örebro University (SE), Skåne University Hospital (SE)
Openalex Percentile: Top 25%
Genomics and Rare Diseases
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