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Executive Function in Fragile X Syndrome: A Systematic Review.
Lauren M Schmitt1, Rebecca C Shaffer2,3, David Hessl4
1Division of Child and Adolescent Psychiatry, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA. lauren.schmitt@cchmc.org.
This review summarizes executive function (EF) deficits in Fragile X syndrome (FXS), highlighting cognitive and biological factors. It aims to improve understanding and identify new treatment targets for FXS.
Area of Science:
- Neuroscience
- Genetics
- Psychology
Background:
- Executive functions (EF) are crucial for goal-directed behavior, encompassing working memory, inhibitory control, and cognitive flexibility.
- Fragile X syndrome (FXS), a leading inherited cause of intellectual disability, is marked by significant EF deficits.
- Existing research necessitates a systematic review to consolidate findings on EF in FXS.
Purpose of the Study:
- To systematically review behavioral studies on EF deficits in individuals with FXS.
- To summarize EF impairments across various domains in males and females with FXS.
- To explore clinical and biological correlates of EF deficits and suggest future research directions.
Main Methods:
- Systematic literature review of performance-based behavioral studies.
- Analysis of studies examining executive function domains in Fragile X syndrome.
- Synthesis of findings related to clinical and biological correlates.
Main Results:
- Fragile X syndrome is associated with notable deficits in executive functions, including working memory and inhibitory control.
- EF impairments in FXS extend beyond general cognitive limitations.
- The review identifies gaps in current research and proposes avenues for future investigation.
Conclusions:
- A comprehensive understanding of EF deficits in FXS is crucial for advancing research.
- Identifying pathophysiological mechanisms underlying EF deficits can inform treatment development.
- This review provides a foundation for developing outcome measures and therapeutic targets for FXS.
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