Skip to main content
AAN.com
Article
May 1, 1994

Specific learning disability in children with neurofibromatosis type 1
Significance of MRI abnormalities

May 1994 issue
44 (5) 878

Abstract

To determine whether previously reported areas of increased T2 signal intensity on MRI examination in children with neurofibromatosis type 1 (NF 1) are associated with deficits in development and learning common in this population, we evaluated 51 children with NF 1 (aged 8 to 16 years). Forty children completed the full assessment protocol (MRI, medical, psychometric, speech therapy, and occupational therapy assessments). The mean Full Scale IQ scores for the entire study population showed a left shift compared with the normal population, and the distribution of IQ scores was bimodal, suggesting that there are two populations of patients with NF 1–those with and those without a variable degree of cognitive impairment. There was no association between lower IQ scores and any clinical variable. Areas of increased T2 signal intensity unidentified bright objects (UBO+) were present in 62.5% of the study population, and their presence was not related to clinical severity, sex, age, socioeconomic status, macrocephaly, or family history of NF 1. However, compared with children without areas of increased T2 signal intensity (UBO-), the UBO+ group had significantly lower mean values for IQ and language scores and significantly impaired visuomotor integration and coordination. Children with areas of increased T2 signal intensity were at a much higher risk for impaired academic achievement. Children without increased T2 signal on MRI (UBO-) did not significantly differ from the general population in any measure of ability or performance. Areas of increased T2 signal on MRI represent dysplastic glial proliferation and aberrant myelination in the developing brain and are associated with deficits in higher cognitive function. The presence of these abnormal signals on MRI divides the NF 1 population into two distinct groups anatomically and developmentally (UBO+ and UBO-). These two groups should be considered separately in the assessment and management of learning disability in children with NF 1.

Get full access to this article

View all available purchase options and get full access to this article.

Information & Authors

Information

Published In

Neurology®
Volume 44Number 5May 1994
Pages: 878
PubMed: 8190291

Publication History

Published online: May 1, 1994
Published in issue: May 1994

Permissions

Request permissions for this article.

Authors

Affiliations & Disclosures

K. North, MBBS
Children's Hospital, Sydney, Australia.
P. Joy, MA, MSc
Children's Hospital, Sydney, Australia.
D. Yuille, BAppSc (Sp Path)
Children's Hospital, Sydney, Australia.
N. Cocks, BAppSc (Occ Ther)
Children's Hospital, Sydney, Australia.
E. Mobbs, MA, BSc
Children's Hospital, Sydney, Australia.
P. Hutchins, MBBS
Children's Hospital, Sydney, Australia.
K. McHugh, MBBS
Children's Hospital, Sydney, Australia.
M. de Silva, MBBS
Children's Hospital, Sydney, Australia.

Metrics & Citations

Metrics

Citation information is sourced from Crossref Cited-by service.

Citations

Download Citations

If you have the appropriate software installed, you can download article citation data to the citation manager of your choice. Select your manager software from the list below and click Download.

Cited By
  1. Modeling neurodegenerative and neurodevelopmental disorders in the Drosophila mushroom body , Learning & Memory, 31, 5, (a053816), (2024).https://doi.org/10.1101/lm.053816.123
    Crossref
  2. Remembering punishment-related odors: Insights from the Drosophila brain and its inspiration, Reference Module in Neuroscience and Biobehavioral Psychology, (2024).https://doi.org/10.1016/B978-0-443-15754-7.00052-3
    Crossref
  3. Neurofibromatosis type1, type 2, tuberous sclerosis and Von Hippel-Lindau disease, Child's Nervous System, 39, 10, (2791-2806), (2023).https://doi.org/10.1007/s00381-023-06160-3
    Crossref
  4. The role of unidentified bright objects in the neurocognitive profile of neurofibromatosis type 1 children: a volumetric MRI analysis, Acta Neurologica Belgica, 124, 1, (223-230), (2023).https://doi.org/10.1007/s13760-023-02381-0
    Crossref
  5. Increased prevalence of brain tumors classified as T2 hyperintensities in neurofibromatosis 1, Neurology Clinical Practice, 8, 4, (283-291), (2023)./doi/10.1212/CPJ.0000000000000494
    Abstract
  6. Motor Function and Physiology in Youth With Neurofibromatosis Type 1, Pediatric Neurology, 143, (34-43), (2023).https://doi.org/10.1016/j.pediatrneurol.2023.02.014
    Crossref
  7. Using a semi-automated approach to quantify Unidentified Bright Objects in Neurofibromatosis type 1 and linkages to cognitive and academic outcomes, Magnetic Resonance Imaging, 98, (17-25), (2023).https://doi.org/10.1016/j.mri.2022.12.022
    Crossref
  8. References, Principles of Cognitive Rehabilitation, (253-354), (2023).https://doi.org/10.1016/B978-0-443-18750-6.00028-6
    Crossref
  9. Electrophysiological and Behavioral Evidence for Hyper- and Hyposensitivity in Rare Genetic Syndromes Associated with Autism, Genes, 13, 4, (671), (2022).https://doi.org/10.3390/genes13040671
    Crossref
  10. Longitudinal Investigation of Early Motor Development in Neurofibromatosis Type 1, Journal of Pediatric Psychology, 47, 2, (180-188), (2021).https://doi.org/10.1093/jpepsy/jsab090
    Crossref
  11. See more
Loading...

View Options

Login options

Check if you have access through your login credentials or your institution to get full access on this article.

Personal login Institutional Login
Purchase Options

The neurology.org payment platform is currently offline. Our technical team is working as quickly as possible to restore service.

If you need immediate support or to place an order, please call or email customer service:

  • 1-800-638-3030 for U.S. customers - 8:30 - 7 pm ET (M-F)
  • 1-301-223-2300 for customers outside the U.S. - 8:30 - 7 pm ET (M-F)
  • [email protected]

We appreciate your patience during this time and apologize for any inconvenience.

View options

PDF and All Supplements

Download PDF and Supplementary Material

Full Text

View Full Text

Figures

Tables

Media

Share

Share

Share article link

Share