Extent of magnitude representation deficit and relationship with arithmetic skills in children with 22q11.2DS

Orphanet J Rare Dis. 2024 Jul 3;19(1):250. doi: 10.1186/s13023-024-03263-1.

Abstract

Background: Previous studies have produced conflicting results concerning the extent of magnitude representation deficit and its relationship with arithmetic achievement in children with 22q11.2 deletion syndrome. More specifically, it remains unclear whether deficits are restricted to visuospatial content or are more general and whether they could explain arithmetical impairment.

Methods: Fifteen 5- to 12-year-old children with 22q11.2 deletion syndrome and 23 age-matched healthy controls performed a non-symbolic magnitude comparison task. Depending on the trial, participants had to compare stimuli with high or low visuospatial load (visuospatial stimuli or temporal sequence of visual stimuli). The participants also completed a battery of arithmetic skills (ZAREKI-R) and a battery of global cognitive functioning (WISC-V or WPPSI-IV), from which working memory and visuospatial indices were derived.

Results: Children with 22q11.2DS responded as fast as healthy controls did but received fewer correct responses, irrespective of visuospatial load. In addition, their performance in the non-symbolic magnitude comparison task did not correlate with the ZAREKI total score, while the working memory index did.

Conclusion: Children with 22q11.2DS might suffer from a global magnitude representation deficit rather than a specific deficit due to visuospatial load. However, this deficit alone does not seem to be related to arithmetic achievement. Working memory might be a better concern of interest in favoring arithmetic skills in patients with 22q11.2 deletion syndrome.

Trial registration: Clinicaltrials, NCT04373226 . Registered 16 September 2020.

Keywords: 22q11.2 deletion syndrome; Arithmetical skills; Magnitude comparison task; Working memory.

Publication types

  • Clinical Study

MeSH terms

  • Child
  • Child, Preschool
  • Cognition / physiology
  • DiGeorge Syndrome* / physiopathology
  • Female
  • Humans
  • Male
  • Mathematics
  • Memory, Short-Term / physiology

Associated data

  • ClinicalTrials.gov/NCT04373226