Visual-spatial performance deficits in children with neurofibromatosis type-1

Gregory W. Schrimsher, Rebecca L. Billingsley, John M. Slopis, Bartlett D. Moore

Research output: Contribution to journalArticlepeer-review

75 Scopus citations

Abstract

Neurofibromatosis type-1 (NF1) is a common genetic disorder associated with a variety of medical complications, cognitive impairments, and behavioral problems including a high incidence of Attention Deficit Hyperactivity Disorder (ADHD). The current study examined the hypotheses that deficits in visual-spatial/motor abilities enable one to discriminate and classify children with NF1 (n = 101) compared to control children (n = 37), beyond effects secondary to parent reported ADHD symptomology. Discriminant analysis showed a multivariate combination of visual-spatial/motor ability tests (Judgment of Line Orientation, Block Design subtest of the WISC-III, Recognition-Discrimination Test, Beery Visual-Motor Integration Test) to be a significant predictor of NF1 diagnostic status (P=0.0000004; canonical R 2 = 0.2306). A significantly greater degree of ADHD behavior was found in the NF1 group, and a discriminant analysis using ADHD residualized visual-spatial motor scores indicated that the combination of tests continued to be a significant predictor of group membership after the level of ADHD behavior was controlled (P = 0.00002 and a canonical R2 = 0.1818). This combination of tests proved to be a strong discriminator of NF1. It correctly identified 90% of individuals with the diagnosis, and may be useful to educators to provide assistance and alternatives to minimize the impact of learning problems in those with either known or suspected NF1.

Original languageEnglish (US)
Pages (from-to)326-330
Number of pages5
JournalAmerican Journal of Medical Genetics
Volume120 A
Issue number3
DOIs
StatePublished - Jul 30 2003

Keywords

  • Attention deficit-hyperactivity disorder
  • Children
  • Neurofibromatosis type-1
  • Visual-motor
  • Visual-spatial

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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