2012
DOI: 10.1016/j.jad.2010.11.025
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Occurrence of affective disorders compared to other psychiatric disorders in children and adolescents with 22q11.2 deletion syndrome

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Cited by 41 publications
(38 citation statements)
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“…As stated previously, specific phobia is the most common anxiety disorder at all ages in our study. These findings were consistent with previous studies [1,3]. Interestingly, OCD occurred rather infrequently compared to the results found in other studies on VCFS [10].…”
Section: Discussionsupporting
confidence: 93%
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“…As stated previously, specific phobia is the most common anxiety disorder at all ages in our study. These findings were consistent with previous studies [1,3]. Interestingly, OCD occurred rather infrequently compared to the results found in other studies on VCFS [10].…”
Section: Discussionsupporting
confidence: 93%
“…This rate is considerably higher than the 5 % estimated prevalence in school age population without VCFS [26]. Interestingly, the rate of depression in our sample is higher than the results reported in some previous studies in youth with VCFS [1,3]. Sample sizes or differences in age ranges could account for some of these differences.…”
Section: Discussioncontrasting
confidence: 83%
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“…These rare syndromes often show up across multiple diagnostic categories, suggesting risk of neurobehavioral impairment that is modified by other developmental, environmental, or genetic factors. For example, deletion of chromosome 22q11.2 results in velocardiofacial syndrome (VCFS), which is associated with diagnosis of intellectual disability, ADHD, and ASD in childhood (Hooper et al, 2013), mood disorders in adolescence (Jolin et al, 2012), and psychosis in adulthood (Green et al, 2009). As an even rarer example, a balanced translocation in one family identified disruption of the DISC1 gene as a highly penetrant risk factor for schizophrenia and mood disorders (Millar et al, 2000).…”
Section: Rare Simple Genetic Phenocopies Could Reveal New Treatment mentioning
confidence: 99%
“…Associations between rare variants and psychiatric phenotypes that have been published so far may reflect this trend. For example, 22q11 deletion was initially found to be overrepresented in patients with schizophrenia, 4 mood disorders, 5 anxiety disorders and attention-deficit/ hyperactivity disorder, 6 pervasive developmental disorders and various levels of intellectual deficit. 5,8,9 The same pattern of indiscriminate association of many psychiatric phenotypes (e.g., mental retardation, schizophrenia, autism) and neurologic disorders (e.g., epilepsy) with chromosomal variants (e.g., translocation disrupting DISC1 [10][11][12][13] ) and copy number variations (CNVs) [14][15][16][17] is increasingly reported as investigators search for these rare variants in patients with various disorders or in carriers of a specific rare variant.…”
Section: Psychiatric Genetic Researchmentioning
confidence: 99%