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
. 2020 Feb 27:11:128.
doi: 10.3389/fneur.2020.00128. eCollection 2020.

Lived Experiences of Fragile X Syndrome Caregivers: A Scoping Review of Qualitative Studies

Affiliations

Lived Experiences of Fragile X Syndrome Caregivers: A Scoping Review of Qualitative Studies

Karen Kengne Kamga et al. Front Neurol. .

Abstract

Fragile X Syndrome (FXS) is the most common x-linked monogenic cause of Intellectual Disability (ID) and Autism Spectrum Disorder (ASD). Taking care of children with ID is challenging and overwhelming due to the multiple facets of caregiving. This scoping review aimed at summarizing the qualitative literature on the experiences of families living with FXS, identify key themes and determine the gaps in the extant literature. We conducted a literature search in May 2019 using four databases; PubMed, Web of Science, African-Wide-Information, and Scopus. The keywords used in our search strategy were associated with caregivers, lived experiences, FXS, and qualitative research. All English language articles with full-text reporting were included. Studies associated with other neurodevelopmental conditions and quantitative studies were excluded. We identified 12 out of 203 articles that described the lived experiences of families with FXS. Most articles originated from the United States of America and mothers were the main caregivers. We summarized our findings into four major themes which are; grief experiences, challenges of living with FXS, coping mechanisms and the need to plan for future outcomes. This scoping review highlights the scarcity of qualitative FXS literature in the African population and frustrations endured by families with FXS due to the low knowledge of FXS by healthcare workers. More research is needed to evaluate the impact of living with FXS in males and fathers.

Keywords: care givers; fragile X syndrome; lived experience; qualitative research; scoping review.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Chart describing the article selection process.
Figure 2
Figure 2
Flow chart describing the lived experiences of families with FXS.

References

    1. Hunter J, Rivero-Arias O, Angelov A, Kim E, Fotheringham I, Leal J. Epidemiology of fragile X syndrome: a systematic review and meta-analysis. Am J Med Genet A. (2014) 164A:1648–58. 10.1002/ajmg.a.36511 - DOI - PubMed
    1. Weiler IJ, Greenough W. Synaptic synthesis of the Fragile X protein: possible involvement in synapse maturation and elimination. Am J Med Genet. (1999) 83:248–52. 10.1002/(SICI)1096-8628(19990402)83:4<;248::AID-AJMG3>;3.0.CO;2-1 - DOI - PubMed
    1. Hagerman RJ, Hendren RL. Treatments of Neurodevelopmental Disorders: Targeting Neurobiological Mechanisms. New York, NY: Oxford University Press (2014). p. 376 10.1093/med/9780199937806.001.0001 - DOI
    1. Peprah E. Fragile X syndrome: the FMR1 CGG repeat distribution among world populations. Ann Hum Genet. (2012) 76:178–91. 10.1111/j.1469-1809.2011.00694.x - DOI - PMC - PubMed
    1. Yim S-Y, Jeon BH, Yang JA, Kim HJ. Fragile X syndrome in Korea: a case series and a review of the literature. J Korean Med Sci. (2008) 23:470–6. 10.3346/jkms.2008.23.3.470 - DOI - PMC - PubMed

Publication types