Cited by 29Genetics and Neurodevelopmental DisordersDown syndrome and intellectual disability researchGenomics and Rare Diseases

Understanding fragile X syndrome

Berry-Kravis, Elizabeth, Grossman, Aaron W., Crnic, Linda S., Greenough, William T.·2002·Current Paediatrics

Integrity signals

Registry

Crossref · 10.1054/cupe.2002.0305

Cites

23 of 23 references verified0 citation errors · 0 not checkable

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  • Relative strengths in Fragile X syndrome include receptive language skills, visual memory, acquisition of factual information, imitation skills and gestalt processing.

    “Relative strengths include receptive language skills, visual memory, acquisition of factual information, imitation skills and gestalt processing (Berry-Kravis et al., 2002).”

    From Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders (2014) · cites this paper as Berry-Kravis et al., 2002

  • Individuals with Fragile X syndrome exhibit deficits in visuospatial tasks, quantitative skills, short-term and working memory, expressive language skills, sequential processing and executive function.

    “FXS individuals exhibit deficits in visuospatial tasks, quantitative skills, short-term and working memory, expressive language skills, sequential processing and executive function (Berry-Kravis et al., 2002; Cornish et al., 1999; Freund and Reiss, 1991; Hall et al., 2012; Kwon et al., 2001; Maes et al., 1994).”

    From Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders (2014) · cites this paper as Berry-Kravis et al., 2002

  • Of individuals with Fragile X syndrome and autistic behaviors, 15-40% of males and a few females meet the diagnostic criteria for ASD.

    “Of the individuals with FXS and autistic behaviors, 15–40% of males and a few females meet the diagnostic criteria for ASD (Berry-Kravis et al., 2002).”

    From Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders (2014) · cites this paper as Berry-Kravis et al., 2002

  • The behavioral and cognitive deficits of Fmr1 KO mice are actually quite subtle and parallel Fragile X syndrome patients.

    “By most accounts Fmr1 KO mice appear to have relatively normal behavior, but research has shown that the behavioral and cognitive deficits of the KO are actually quite subtle and parallel FXS patients (Berry-Kravis et al., 2002; D’Hooge et al., 1997; Paradee et al., 1999; Peier et al., 2000).”

    From Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders (2014) · cites this paper as Berry-Kravis et al., 2002

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Authors
Berry-Kravis, E., Grossman, A. W., Crnic, L. S., & Greenough, W. T.
Affiliations
  • University of Illinois Urbana-Champaign (US)
  • University of Colorado Anschutz (US)
Venue
Current Paediatrics
Publisher
Elsevier BV
Published
2002-08
Volume
12
Issue
4
Pages
316-324
ISSN
0957-5839 (ISSN-L)
OpenAlex
W2079802852
Cited by
29
References
23
Citations by year
2023: 1 · 2020: 1 · 2018: 3 · 2017: 2 · 2016: 2 · 2015: 4 · 2014: 4 · 2012: 3
FWCI
0.35
Type
journal article
Language
en
Open access
closed
Locations
Current Paediatrics (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Down syndrome and intellectual disability research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
Keywords
fragile X syndrome, FMRP, intellectual disability, hyperactivity, anxiety, mitral valve prolapse, gastroesophageal reflux, otitis media, genetic counseling, behavior management

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