BACKGROUND AND PURPOSE: MR imaging studies and neuropathologic findings in
individuals with 22q11. 2 deletion syndrome show anomalous early brain development. We …

Abstract Background 22q11. 2 Deletion Syndrome (22q11DS) is a genetic,
neurodevelopmental disorder characterized by a chromosomal deletion and a distinct …

BACKGROUND AND PURPOSE: The 22q11. 2 deletion syndrome is a common genetic
microdeletion syndrome that results in cognitive delays and an increased risk of several …

22q11 deletion syndrome (22q11DS) is a common genetic condition associated with
learning disability and high risk for psychiatric illness, in particular schizophrenia. Previous …

Background There is increased risk of developing psychosis in 22q11. 2 deletion syndrome
(22q11DS). Although this condition is associated with morphologic brain abnormalities …

22q11. 2 deletion syndrome (22q11. 2DS) is a common genetic disorder with enormous
phenotypic heterogeneity. Despite the established prevalence of developmental and …

Chromosome 22q11. 2 deletion syndrome (22q11DS) is associated with cognitive deficits
and morphometric brain abnormalities in childhood and a markedly elevated risk of …

In people with velo-cardio-facial syndrome [or 22q11. 2 deletion syndrome (22qDS)], a
single interstitial deletion of chromosome 22q11. 2 causes a wide spectrum of cognitive …

22q11. 2 Deletion Syndrome is associated with cognitive, behavioural, and psychiatric
problems and is known to affect brain structure. Recently, 22q11. 2 Deletion Syndrome has …

Abstract The 22q11. 2 deletion syndrome (22qDS) is the most common microdeletion
syndrome in humans. Its multisystem manifestations include congenital anomalies and …