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Published on: April 22, 2015
Developmental trajectories and correlates of sensory processing in young boys with fragile X syndrome
Grace T Baranek1, Jane E Roberts, Fabian J David
1Division of Occupational Science, Department of Allied Health Sciences, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA. gbaranek@med.unc.edu
Insights
Sensory processing issues in fragile X syndrome (FXS) emerge early and worsen through preschool. Early intervention for these sensory challenges in children with FXS is crucial.
Area of Science:
- Neurodevelopmental disorders
- Pediatric sensory processing
- Fragile X syndrome research
Background:
- Fragile X syndrome (FXS) is a genetic disorder associated with developmental challenges.
- Longitudinal data on sensory processing development in FXS is lacking.
- Understanding sensory processing trajectories is vital for early intervention.
Purpose of the Study:
- To investigate the developmental trajectories of sensory processing in boys with FXS from infancy to preschool.
- To identify correlates of sensory processing differences in this population.
- To establish a baseline for future FXS sensory processing research.
Main Methods:
- Longitudinal study design involving 13 boys with FXS.
- Data collected 2-6 times between 9 and 54 months of age.
- Utilized observational and parent-report measures for sensory processing assessment.
Main Results:
- An increasing number of boys with FXS showed atypical sensory processing over time.
- Observational methods were more sensitive than parent reports in early infancy.
- Developmental quotient and age predicted hyporesponsiveness; hyperresponsiveness tended to increase with age.
Conclusions:
- Sensory processing deficits in FXS are evident early and escalate through preschool years.
- Early identification and intervention strategies are recommended to mitigate long-term impacts.
- Findings highlight the need for targeted support for sensory needs in children with FXS.
Background And Purpose:
No longitudinal study on sensory processing in children with fragile X syndrome (FXS) exists. This study examined developmental trajectories and correlates of sensory processing from infancy through preschool years in 13 boys with FXS.
Method:
Participants were assessed using observational and parent-report measures 2-6 times between 9 and 54 months of age.
Results:
Over time, an increasing proportion of boys displayed sensory processing that differed significantly from test norms. Observational measures were more sensitive than parent-reports early in infancy. Age and developmental quotient significantly predicted levels of hyporesponsiveness; there was a trend for hyperresponsiveness to increase with age. Baseline physiological and biological measures were not predictive.
Conclusions:
Sensory processing problems are observable early and grow increasingly problematic from infancy through the preschool ages. Early identification and intervention may attenuate long-term difficulties for children with FXS.
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