A new window on neurocognitive dysfunction in the childhood form of myotonic dystrophy type 1 (DM1)

Neuromuscul Disord. 2011 Jul;21(7):468-76. doi: 10.1016/j.nmd.2011.04.009. Epub 2011 May 17.

Abstract

Not much is known about the neurocognitive deficits in the childhood phenotypic expression of DM1. Twenty-four children and adolescents with no mental retardation were administered an extensive neuropsychological battery to investigate cognition in terms of memory, executive functions and visuo-spatial abilities. The results showed discrepancies between Wechsler's indexes with higher scores in Verbal Comprehension than Perceptive Organization and Speed of Processing. Memory assessment using Signoret's Memory Battery revealed a clear difference between verbal and visuospatial memory but no impairment between short and long-term memory. Concerning executive abilities, DM1 subjects showed greater deficits in processing speed than in mental flexibility, inhibition or working memory. This pattern of deficits could implicate a frontoparietal circuit in accordance with the neural networks involved in the adult form of DM1 and reopens the question of a continuum between childhood and adulthood neurocognitive impairments.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Child
  • Cognition Disorders / complications
  • Cognition Disorders / psychology*
  • Executive Function / physiology
  • Female
  • Humans
  • Inhibition, Psychological
  • Male
  • Memory / physiology
  • Myotonic Dystrophy / complications
  • Myotonic Dystrophy / psychology*
  • Neuropsychological Tests