Lower Prepulse Inhibition in Children With the 22q11 Deletion Syndrome
نویسندگان
چکیده
منابع مشابه
Lower prepulse inhibition in children with the 22q11 deletion syndrome.
OBJECTIVE The 22q11 deletion syndrome is associated with a range of possible physical anomalies, probable ongoing learning disabilities, and a specific constellation of neuropsychological deficits, including impairments in selective and executive visual attention, working memory, and sensorimotor functioning. It has been estimated that 25% of the children with 22q11 deletion syndrome go on to d...
متن کاملNetworks of attention in children with the 22q11 deletion syndrome.
The 22q11 chromosomal deletion syndrome (22q11 DS) is associated with learning disabilities and a complex neuropsychological profile. Previous findings have suggested that executive attention deficits might underlie other neurocognitive anomalies. We administered the child Attention Network Test (ANT) to 52 children ages 5.0 to 11.5, 32 22q11 DS children (19 girls) and 20 controls (13 girls) an...
متن کاملNeuromotor deficits in children with the 22q11 deletion syndrome.
The 22q11 chromosomal deletion syndrome (22q11DS) is associated with a heterogeneous physical phenotype, neurocognitive deficits, and increased risk of later psychiatric illness. Sporadic clinical reports suggested motor differences, but quantitative studies of movement in children with 22q11DS are rare. If present in a majority of affected school-age children, characterization of neuromotor de...
متن کاملOlfactory disorder in children with 22q11 deletion syndrome.
OBJECTIVE 22q11 deletion syndrome, a common human interstitial deletion syndrome (1:5000), is associated with a heterogeneous physical phenotype, including several factors that markedly increase the risk for olfactory disorder. Despite its potential consequences, pediatric studies of impaired olfaction are rare, and odor detection in children with 22q11 deletion syndrome has not yet been examin...
متن کامل22q11 Deletion Syndrome with Vascular Anomalies
DiGeorge syndrome, also termed 22q11.2 deletion syndrome, represents a spectrum of disorders that include thymic aplasia/hypoplasia, parathyroid aplasia/hypoplasia, conotruncal vascular anomalies, and velocardiofacial (Shprintzen) syndrome. This case report describes a novel constellation of cardiovascular anomalies in a 31-year-old patient with 22q11.2 deletion confirmed by fluorescence in sit...
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ژورنال
عنوان ژورنال: American Journal of Psychiatry
سال: 2005
ISSN: 0002-953X,1535-7228
DOI: 10.1176/appi.ajp.162.6.1090