Children and adolescents with neurofibromatosis 1: a behavioral phenotype

J Dev Behav Pediatr. 1996 Aug;17(4):229-39.

Abstract

Twenty 6- to 17-year-old children with neurofibromatosis 1. (NF1) were compared to 20 age- and sex-matched siblings on a wide range of neuropsychological and behavioral dimensions. In familial cases, diagnostic status was confirmed by gene linkage with greater than 98% accuracy. Visual examinations that included assessments of visual evoked responses (VER) were performed on subjects with NF1. Forty-two percent of NF1 subjects had abnormal VER and underwent magnetic resonance imagery or computed tomography scans of the brain. On a variety of skills, subjects with NF1 performed more poorly than unaffected siblings. Children with NF1 were found to be less competent on measures of cognitive, language, and motor development, visual-spatial judgment, visual-motor integration, and academic achievement. Learning disabilities were common in children with NF1. Parents and teachers reported that NF1 subjects had internalizing problems and difficulty interacting with peers. A behavioral phenotype for NF1 and recommendations for preventative interventions are proposed.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adolescent
  • Brain / physiopathology
  • Child
  • Child Behavior Disorders / genetics*
  • Child Behavior Disorders / physiopathology
  • Child Behavior Disorders / psychology
  • Developmental Disabilities / genetics*
  • Developmental Disabilities / physiopathology
  • Developmental Disabilities / psychology
  • Female
  • Genetic Linkage / genetics
  • Humans
  • Internal-External Control
  • Learning Disabilities / genetics
  • Learning Disabilities / physiopathology
  • Learning Disabilities / psychology
  • Male
  • Neurofibromatosis 1 / genetics*
  • Neurofibromatosis 1 / physiopathology
  • Neurofibromatosis 1 / psychology
  • Neurologic Examination
  • Neuropsychological Tests
  • Personality Assessment
  • Phenotype*