Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Observational Study
. 2025 Aug;28(4):e70340.
doi: 10.1111/hex.70340.

Identifying the Impacts, Obstacles and Information Barriers for Parents of Children Living With Genetic Neurodevelopmental Disorders: A Qualitative Study

Collaborators, Affiliations
Observational Study

Identifying the Impacts, Obstacles and Information Barriers for Parents of Children Living With Genetic Neurodevelopmental Disorders: A Qualitative Study

Karen J Low et al. Health Expect. 2025 Aug.

Abstract

Background: A genetic neurodevelopmental disorder (GND) impacts all aspects of a child's and family's life. GNDs are rare; most have limited natural history data. We aimed to understand the impacts, obstacles, information barriers and coping strategies developed through parents' experience of receiving and living with a child's diagnosis.

Design and participants: This analysis is part of the UK multicentre observational study of children with rare GNDs (GenROC). We conducted 17 semi-structured online interviews with parents of children with GNDs (aged 0-15 years) from November 2023 to March 2024. Data were analysed following the principles of thematic analysis.

Results: We identified five themes. (1) Impact on the family around a genetic diagnosis: Distress begins well before a diagnosis is received; there is an impact upon the receipt itself and the ongoing impact on the family thereafter. (2) Impact of uncertainty, lack of data and 'rareness'. The experience of parenting when so little is known about your child's condition. (3) Relationships with health professionals. Positive where parents are empowered and feel part of the team; negative where parents feel not heard/believed due to a professional lack of expertise/understanding. (4) Parent mental health: GNDs can be a significant burden to family life. The need to advocate for services has a negative impact. Feelings of isolation through rareness. (5) Coping strategies and factors that help: Support/Facebook groups are considered highly beneficial. Parents develop new positive identities, including that of advocate, professional and educator.

Conclusions: GNDs represent a major challenge for families, clinicians and service providers. Distressed parents are struggling to cope with challenges and suffer from poor mental health. Psychosocial support, better signposting and health professional education may help.

Patient contribution: Patient Participant Involvement group (comprising five mothers and one father of children with varying GNDs, one young person with a GND, and one genetics family charity representative) contributed to topic guide development and methodology and provided feedback on results.

Keywords: distress; genomics; parent; rare.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Summary of themes.
Figure 2
Figure 2
Implications for practice.

References

    1. Wright C. F., Campbell P., Eberhardt R. Y., et al., “Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland,” New England Journal of Medicine 388, no. 17 (2023): 1559–1571. - PMC - PubMed
    1. Copeland H., Low K. J., Wynn S. L., et al., “Large‐Scale Evaluation of Outcomes After a Genetic Diagnosis in Children With Severe Developmental Disorders,” Genetics in Medicine Open 2 (2024): 101864. - PMC - PubMed
    1. NHS. 2024. National Genomic Test Directory: Testing Criteria for Rare and Inherited Disease.
    1. Peter M., Hammond J., Sanderson S. C., et al., “Participant Experiences of Genome Sequencing for Rare Diseases in the 100,000 Genomes Project: A Mixed Methods Study,” European Journal of Human Genetics 30, no. 5 (2022): 604–610. - PMC - PubMed
    1. Aldridge C. E., Osiovich H., (Hal) Siden H., and Elliott A. M., “Rapid Genome‐Wide Sequencing in a Neonatal Intensive Care Unit: A Retrospective Qualitative Exploration of Parental Experiences,” Journal of Genetic Counseling 30, no. 2 (2021): 616–629. - PubMed

Publication types