Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Memory abilities in children with Williams syndrome

S Vicari1, D Brizzolara, G A Carlesimo

  • 1IRCCS Ospedale Pediatrico Bambino Gesù, Santa Marinella, Roma.

Cortex; a Journal Devoted to the Study of the Nervous System and Behavior
|September 1, 1996
PubMed
Summary

Children with Williams syndrome (WS) exhibit impaired visuo-spatial memory and long-term verbal learning deficits. This highlights specific cognitive disruptions in intellectual disability, impacting memory functions differently.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Psychological predictors of disease flares in pediatric inflammatory bowel disease: a prospective study.

Psychology, health & medicine·2026
Same author

The transdiagnostic role of emotional dysregulation and temperament in non suicidal self-injury: Cross sectional study among adolescents receiving intensive psychiatric care.

Psychiatry research·2026
Same author

Abnormal Forgetting Rate from the Recency Portion of a Word-List in Patients with Subjective Cognitive Decline.

Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists·2025
Same author

Case Report: Diagnostic assessment, developmental trajectory and treatment approaches in a case of a complex neurodevelopmental syndrome associated with non- synonymous variants in <i>MECP2</i> (p. R133C) and <i>GABBR1</i>.

Frontiers in pediatrics·2025
Same author

Family functioning and eating psychopathology in developmental restrictive eating disorders after Covid-19 lockdown.

Eating and weight disorders : EWD·2025
Same author

Characterising repetitive behaviours in children and adolescents with Down syndrome.

Journal of intellectual disability research : JIDR·2024

Area of Science:

  • Neuroscience
  • Genetics
  • Developmental Psychology

Background:

  • Williams syndrome (WS) is a rare genetic disorder associated with intellectual disability, distinct facial features, and medical issues.
  • A hypothesized neuropsychological profile in WS involves relatively preserved language but impaired visuo-spatial abilities.
  • Memory function in WS requires further investigation to fully understand the neurocognitive profile.

Purpose of the Study:

  • To investigate verbal and spatial memory in children with Williams syndrome.
  • To compare the memory performance of WS patients with typically developing children.
  • To elucidate the specific memory deficits contributing to the WS neurocognitive profile.

Main Methods:

  • Assessed verbal and spatial span in 16 WS patients and controls.

Related Experiment Videos

  • Evaluated immediate and delayed recall of verbal and visuo-perceptual materials.
  • Utilized comparative analysis between WS group and typically developing children.
  • Main Results:

    • WS children demonstrated significant deficits in visuo-spatial memory across short-term and long-term domains.
    • A dissociation was observed: normal short-term verbal learning but deficient long-term verbal learning in WS patients.
    • Performance differences highlight specific cognitive impairments in WS.

    Conclusions:

    • Intellectual disability in WS is linked to the disrupted functioning of complex cognitive systems.
    • Memory deficits, particularly in visuo-spatial domains, are characteristic of Williams syndrome.
    • Findings support a model where cognitive competencies are differentially affected in intellectual disability.