Psychiatric and cognitive phenotype of childhood myotonic dystrophy type 1

Dev Med Child Neurol. 2012 Oct;54(10):905-11. doi: 10.1111/j.1469-8749.2012.04379.x. Epub 2012 Aug 3.

Abstract

Aim: To investigate the psychiatric and cognitive phenotype in young individuals with the childhood form of myotonic dystrophy type 1 (DM1).

Method: Twenty-eight individuals (15 females, 13 males) with childhood DM1 (mean age 17y, SD 4.6, range 7-24y) were assessed using standardized instruments and cognitive testing of general intelligence, visual attention, and visual-spatial construction abilities.

Results: Nineteen patients had repeated a school grade. The mean (SD) Full-scale IQ was 73.6 (17.5) and mean Verbal IQ was significantly higher than the mean Performance IQ: 80.2 (19.22) versus 72.95 (15.58), p=0.01. Fifteen patients had one or more diagnoses on the DSM-IV axis 1, including internalizing disorders (phobia, n=7; mood disorder, n=6; other anxiety disorders, n=5) and attention-deficit-hyperactivity disorder, inattentive subtype (n=8). Twelve out of 22 patients had alexithymia (inability to express feelings with words and to recognize and share emotional states). Cognitive testing found severe impairments in visual attention and visual-spatial construction abilities in four out of 18, and 14 out of 24 patients respectively. No diagnosis was correlated with the transmitting parent's sex or with cytosine-thymine-guanine (CTG) repeat numbers. Patients with severe visual-spatial construction disabilities had a significantly longer CTG expansion size than those with normal visual-spatial abilities (p=0.04).

Interpretation: Children and adolescents with childhood DM1 have frequent diagnoses on DSM-IV axis 1, with internalizing disorders being the most common type of disorder. They also have borderline low intelligence and frequent impairments in attention and visual-spatial construction abilities.

Publication types

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

MeSH terms

  • Adolescent
  • Attention
  • Child
  • Cognition Disorders / diagnosis*
  • Cognition Disorders / genetics*
  • Comorbidity
  • DNA Mutational Analysis
  • Female
  • Humans
  • Intelligence / genetics
  • Male
  • Mental Disorders / diagnosis*
  • Mental Disorders / genetics*
  • Myotonic Dystrophy / diagnosis*
  • Myotonic Dystrophy / genetics*
  • Pattern Recognition, Visual
  • Phenotype*
  • Psychomotor Performance
  • Trinucleotide Repeat Expansion / genetics
  • Young Adult