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

Authors :
Van Aken K
De Smedt B
Van Roie A
Gewillig M
Devriendt K
Fryns JP
Simons J
Swillen A
Source :
Developmental Medicine & Child Neurology. Mar2007, Vol. 49 Issue 3, p210-213. 4p.
Publication Year :
2007

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00121622
Volume :
49
Issue :
3
Database :
Academic Search Index
Journal :
Developmental Medicine & Child Neurology
Publication Type :
Academic Journal
Accession number :
106006781
Full Text :
https://doi.org/10.1111/j.1469-8749.2007.00210.x