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Observations on intelligence and behavior in 15 patients with Legius syndrome.

Authors :
Denayer E
Descheemaeker MJ
Stewart DR
Keymolen K
Plasschaert E
Ruppert SL
Snow J
Thurm AE
Joseph LA
Fryns JP
Legius E
Source :
American journal of medical genetics. Part C, Seminars in medical genetics [Am J Med Genet C Semin Med Genet] 2011 May 15; Vol. 157C (2), pp. 123-8. Date of Electronic Publication: 2011 Apr 14.
Publication Year :
2011

Abstract

Legius syndrome is a RAS-MAPK syndrome characterized by pigmentary findings similar to neurofibromatosis type 1 (NF1), but without tumor complications. Learning difficulties and behavioral problems have been reported to be associated with Legius syndrome, but have not been studied systematically. We investigated intelligence and behavior in 15 patients with Legius syndrome and 7 unaffected family members. We report a mean full-scale IQ of 101.57 in patients with Legius syndrome, which does not differ from the control group. We find a significantly lower Performance IQ in children with Legius syndrome compared to their unaffected family members. Few behavioral problems are present as assessed by the Child Behavior Checklist (CBCL) questionnaire. Our observations suggest that, akin to the milder somatic phenotype, the cognitive phenotype in Legius syndrome is less severe than that of NF1.<br /> (2011 Wiley-Liss, Inc.)

Details

Language :
English
ISSN :
1552-4876
Volume :
157C
Issue :
2
Database :
MEDLINE
Journal :
American journal of medical genetics. Part C, Seminars in medical genetics
Publication Type :
Academic Journal
Accession number :
21495177
Full Text :
https://doi.org/10.1002/ajmg.c.30297