Cited by 255Genetics and Neurodevelopmental DisordersDown syndrome and intellectual disability researchAutism Spectrum Disorder Research

Fragile X syndrome: a review of associated medical problems

Kidd, Sharon A., Lachiewicz, Ave, Barbouth, Deborah, Blitz, Robin K., Delahunty, Carol, McBrien, Dianne, Visootsak, Jeannie, Berry-Kravis, Elizabeth·2014·Pediatrics

Abstract

Fragile X syndrome (FXS) is the most common known genetic cause of inherited intellectual disability and the most common known single-gene cause of autism spectrum disorder. It has been reported that a spectrum of medical problems are commonly experienced by people with FXS, such as otitis media, seizures, and gastrointestinal problems. Previous studies examining the prevalence of medical problems related to FXS have been challenging to interpret because of their marked differences in population, setting, and sampling. Through this comprehensive review, we update the literature by reviewing studies that have reported on prominent medical problems associated with FXS. We then compare prevalence results from those studies with results from a large cross-sectional database consisting of data collected by fragile X clinics that specialize in the care of children with FXS and are part of the Fragile X Clinical and Research Consortium. It is vital for pediatricians and other clinicians to be familiar with the medical problems related to FXS so that affected patients may receive proper diagnosis and treatment; improved care may lead to better quality of life for these patients and their families.

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Crossref · 10.1542/peds.2013-4301

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  • FXS is a relatively common inherited intellectual disability often associated with ASD symptoms including perseverative behaviors, speech and sensory difficulties, and disrupted sleep.

    “This relatively common form of inherited intellectual disability is often associated with symptoms of ASD, including perseverative behaviors, speech and sensory difficulties, and disrupted sleep (Kidd et al., 2014).”

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References 97 · Cited by 255

Authors
Kidd, S. A., Lachiewicz, A., Barbouth, D., Blitz, R. K., Delahunty, C., McBrien, D., Visootsak, J., & Berry-Kravis, E.
Affiliations
  • National Fragile X Foundation (US)
  • Duke University (US)
  • University of Miami (US)
  • Barrow Neurological Institute (US)
  • Cleveland Clinic (US)
  • University of Iowa (US)
  • Emory University (US)
  • Departments of Pediatrics,
Venue
Pediatrics
Published
2014-11-01
Volume
134
Issue
5
Pages
995-1005
ISSN
  • 0031-4005 (ISSN-L)
  • 1098-4275
OpenAlex
W2168353812
Cited by
255
References
97
Citations by year
2026: 5 · 2025: 16 · 2024: 19 · 2023: 25 · 2022: 22 · 2021: 23 · 2020: 23 · 2019: 29 · 2018: 19 · 2017: 26 · 2016: 22 · 2015: 23 · 2014: 2
FWCI
3.23
Type
journal article
Language
en
Open access
closed
Locations
  • PEDIATRICS (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Fragile X Foundation
  • Centers for Disease Control and Prevention (5u19dd000753-02, 5U01DD000231)
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 › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
Keywords
fragile X syndrome, comorbidities, otitis media, seizures, gastrointestinal problems, intellectual disability, autism spectrum disorder, prevalence, pediatric care
MeSH terms
Child Development Disorders, Pervasive, Fragile X Syndrome, Gastrointestinal Diseases, Heart Diseases, Humans, Nervous System Malformations, Quality of Life, Seizures

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