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Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects

Authors :
Sólveig Óskarsdóttir
Lena Niklasson
Peder Rasmussen
Christopher Gillberg
Source :
Developmental Medicine & Child Neurology. 44:44-50
Publication Year :
2007
Publisher :
Wiley, 2007.

Abstract

Twenty children and young adults (age range 5 to 33 years, 12 females and eight males) with genetically confirmed 22q11 deletion syndrome (CATCH 22: Cardiac anomaly, Anomalous face, Thymus hypoplasia/aplasia, Cleft palate, and Hypocalcaemia), recruited from a large ongoing study, were given comprehensive assessments with a view to determining the pattern of neuropsychiatric and neuropsychological deficits thought to be part of the syndrome in many cases. IQ ranged between 46 and 100 with a mean score of 70. Half the group had an IQ

Details

ISSN :
14698749 and 00121622
Volume :
44
Database :
OpenAIRE
Journal :
Developmental Medicine & Child Neurology
Accession number :
edsair.doi.dedup.....1bafad78c19a80fce26e10e7d5cff3a2