Motor development in school-aged children with 22q11 deletion (velocardiofacial/DiGeorge syndrome)

Dev Med Child Neurol. 2007 Mar;49(3):210-3. doi: 10.1111/j.1469-8749.2007.00210.x.

Abstract

The aim of this study was to compare the motor development of primary school children (age 5-14y) with a 22q11 deletion (del22q11) group and a control group. The effects of a congenital heart defect (CHD) and IQ on motor development were additionally studied within the del22q11 group. Motor development of 37 children with a del22q11 (20 males, 17 females; mean age 9y 4mo, range 5y 9mo-13y 3mo) and 34 controls (23 males, 11 females; mean age 9y 1mo, range 4y 8mo-13y 6mo) was assessed with the Bruininks-Oseretsky Test of Motor Proficiency. The del22q11 group showed a significant deficit in motor functioning compared with the control group (p < 0.01). Within the del22q11 group there was a significant effect of IQ on motor performance, but no effect of CHD was found. To conclude, primary school children with a del22q11 syndrome showed a significant deficit in motor performance compared with a control group. A significant effect of IQ on motor performance in del22q11 was found.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Analysis of Variance
  • Case-Control Studies
  • Child
  • Child Development / physiology*
  • Chromosomes, Human, Pair 22*
  • Cognition Disorders / diagnosis
  • Cognition Disorders / etiology
  • Cognition Disorders / genetics
  • DiGeorge Syndrome / complications*
  • DiGeorge Syndrome / genetics
  • Female
  • Gene Deletion
  • Heart Defects, Congenital / complications
  • Heart Defects, Congenital / genetics
  • Humans
  • Intelligence / genetics
  • Male
  • Motor Skills / physiology*
  • Motor Skills Disorders / diagnosis
  • Motor Skills Disorders / etiology*
  • Motor Skills Disorders / genetics