Psychosis in children with velocardiofacial syndrome (22q11.2 deletion syndrome)
Velocardiofacial syndrome, now known as 22q11.2 deletion syndrome (22qDS), is estimated to affect more than 700 children born in the United States each year. Some clinical studies have found increased rates of schizophrenia in adults with 22qDS. However, these studies have been limited by small samp...
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Veröffentlicht in: | Current psychiatry reports 2009-04, Vol.11 (2), p.99-105 |
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description | Velocardiofacial syndrome, now known as 22q11.2 deletion syndrome (22qDS), is estimated to affect more than 700 children born in the United States each year. Some clinical studies have found increased rates of schizophrenia in adults with 22qDS. However, these studies have been limited by small sample size and possible ascertainment bias. The psychiatric disorders most commonly reported in children and adolescents with 22qDS have been attention-deficit/hyperactivity disorder, oppositional defiant disorder, anxiety disorders, and major depression. Psychotic symptoms have been observed in 14% to 28% of children with 22qDS, but their clinical significance remains uncertain. A 5-year follow-up study of 22qDS children who reported psychotic symptoms at baseline found they had an increased risk for a subsequent psychotic disorder. Thus, a broad differential diagnosis should be considered when 22qDS children present with psychotic symptoms. Longitudinal studies are needed to better understand the full extent of the psychopathology associated with 22qDS. |
doi_str_mv | 10.1007/s11920-009-0016-y |
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Some clinical studies have found increased rates of schizophrenia in adults with 22qDS. However, these studies have been limited by small sample size and possible ascertainment bias. The psychiatric disorders most commonly reported in children and adolescents with 22qDS have been attention-deficit/hyperactivity disorder, oppositional defiant disorder, anxiety disorders, and major depression. Psychotic symptoms have been observed in 14% to 28% of children with 22qDS, but their clinical significance remains uncertain. A 5-year follow-up study of 22qDS children who reported psychotic symptoms at baseline found they had an increased risk for a subsequent psychotic disorder. Thus, a broad differential diagnosis should be considered when 22qDS children present with psychotic symptoms. Longitudinal studies are needed to better understand the full extent of the psychopathology associated with 22qDS.</description><identifier>ISSN: 1523-3812</identifier><identifier>EISSN: 1535-1645</identifier><identifier>DOI: 10.1007/s11920-009-0016-y</identifier><identifier>PMID: 19302762</identifier><language>eng</language><publisher>New York: Current Science Inc</publisher><subject>Child ; Chromosome Deletion ; Chromosomes, Human, Pair 22 - genetics ; DiGeorge Syndrome - epidemiology ; DiGeorge Syndrome - genetics ; Humans ; Medicine ; Medicine & Public Health ; Psychiatry ; Psychosis ; Psychotic Disorders - epidemiology</subject><ispartof>Current psychiatry reports, 2009-04, Vol.11 (2), p.99-105</ispartof><rights>Current Medicine Group, LLC 2009</rights><rights>Current Medicine Group, LLC 2009.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-8d824b982569fd2e8583a145344e97c2bf43d03881b92d849fb4dee9824fa5bd3</citedby><cites>FETCH-LOGICAL-c370t-8d824b982569fd2e8583a145344e97c2bf43d03881b92d849fb4dee9824fa5bd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11920-009-0016-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11920-009-0016-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19302762$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jolin, Edith M.</creatorcontrib><creatorcontrib>Weller, Ronald A.</creatorcontrib><creatorcontrib>Weller, Elizabeth B.</creatorcontrib><title>Psychosis in children with velocardiofacial syndrome (22q11.2 deletion syndrome)</title><title>Current psychiatry reports</title><addtitle>Curr Psychiatry Rep</addtitle><addtitle>Curr Psychiatry Rep</addtitle><description>Velocardiofacial syndrome, now known as 22q11.2 deletion syndrome (22qDS), is estimated to affect more than 700 children born in the United States each year. Some clinical studies have found increased rates of schizophrenia in adults with 22qDS. However, these studies have been limited by small sample size and possible ascertainment bias. The psychiatric disorders most commonly reported in children and adolescents with 22qDS have been attention-deficit/hyperactivity disorder, oppositional defiant disorder, anxiety disorders, and major depression. Psychotic symptoms have been observed in 14% to 28% of children with 22qDS, but their clinical significance remains uncertain. A 5-year follow-up study of 22qDS children who reported psychotic symptoms at baseline found they had an increased risk for a subsequent psychotic disorder. Thus, a broad differential diagnosis should be considered when 22qDS children present with psychotic symptoms. Longitudinal studies are needed to better understand the full extent of the psychopathology associated with 22qDS.</description><subject>Child</subject><subject>Chromosome Deletion</subject><subject>Chromosomes, Human, Pair 22 - genetics</subject><subject>DiGeorge Syndrome - epidemiology</subject><subject>DiGeorge Syndrome - genetics</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Psychiatry</subject><subject>Psychosis</subject><subject>Psychotic Disorders - epidemiology</subject><issn>1523-3812</issn><issn>1535-1645</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kM9LwzAUx4Mobk7_AC9S8KKHzOQlbZOjDH_BwB30HNomdRldsyWd0v_ejA538vB4D973B3wQuqZkSgnJHwKlEggmRMahGe5P0JimLMU04-np_gaGmaAwQhchrAgBQgScoxGVjECewRgtFqGvli7YkNg2qZa20d60yY_tlsm3aVxVeG1dXVS2aJLQt9q7tUnuALaUTiHRpjGdde3f6_4SndVFE8zVYU_Q5_PTx-wVz99f3maPc1yxnHRYaAG8lALSTNYajEgFKyhPGedG5hWUNWeaMCFoKUELLuuSa2OigddFWmo2QbdD7sa77c6ETq3czrexUgEHkIRlcSaIDqrKuxC8qdXG23Xhe0WJ2jNUA0MVGao9Q9VHz80heVeujT46DtCiAAZBiK_2y_hj9f-pvzt5e3s</recordid><startdate>20090401</startdate><enddate>20090401</enddate><creator>Jolin, Edith M.</creator><creator>Weller, Ronald A.</creator><creator>Weller, Elizabeth B.</creator><general>Current Science Inc</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>M2M</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope></search><sort><creationdate>20090401</creationdate><title>Psychosis in children with velocardiofacial syndrome (22q11.2 deletion syndrome)</title><author>Jolin, Edith M. ; Weller, Ronald A. ; Weller, Elizabeth B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-8d824b982569fd2e8583a145344e97c2bf43d03881b92d849fb4dee9824fa5bd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Child</topic><topic>Chromosome Deletion</topic><topic>Chromosomes, Human, Pair 22 - genetics</topic><topic>DiGeorge Syndrome - epidemiology</topic><topic>DiGeorge Syndrome - genetics</topic><topic>Humans</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Psychiatry</topic><topic>Psychosis</topic><topic>Psychotic Disorders - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jolin, Edith M.</creatorcontrib><creatorcontrib>Weller, Ronald A.</creatorcontrib><creatorcontrib>Weller, Elizabeth B.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Psychology Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><jtitle>Current psychiatry reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jolin, Edith M.</au><au>Weller, Ronald A.</au><au>Weller, Elizabeth B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Psychosis in children with velocardiofacial syndrome (22q11.2 deletion syndrome)</atitle><jtitle>Current psychiatry reports</jtitle><stitle>Curr Psychiatry Rep</stitle><addtitle>Curr Psychiatry Rep</addtitle><date>2009-04-01</date><risdate>2009</risdate><volume>11</volume><issue>2</issue><spage>99</spage><epage>105</epage><pages>99-105</pages><issn>1523-3812</issn><eissn>1535-1645</eissn><abstract>Velocardiofacial syndrome, now known as 22q11.2 deletion syndrome (22qDS), is estimated to affect more than 700 children born in the United States each year. Some clinical studies have found increased rates of schizophrenia in adults with 22qDS. However, these studies have been limited by small sample size and possible ascertainment bias. The psychiatric disorders most commonly reported in children and adolescents with 22qDS have been attention-deficit/hyperactivity disorder, oppositional defiant disorder, anxiety disorders, and major depression. Psychotic symptoms have been observed in 14% to 28% of children with 22qDS, but their clinical significance remains uncertain. A 5-year follow-up study of 22qDS children who reported psychotic symptoms at baseline found they had an increased risk for a subsequent psychotic disorder. Thus, a broad differential diagnosis should be considered when 22qDS children present with psychotic symptoms. Longitudinal studies are needed to better understand the full extent of the psychopathology associated with 22qDS.</abstract><cop>New York</cop><pub>Current Science Inc</pub><pmid>19302762</pmid><doi>10.1007/s11920-009-0016-y</doi><tpages>7</tpages></addata></record> |
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subjects | Child Chromosome Deletion Chromosomes, Human, Pair 22 - genetics DiGeorge Syndrome - epidemiology DiGeorge Syndrome - genetics Humans Medicine Medicine & Public Health Psychiatry Psychosis Psychotic Disorders - epidemiology |
title | Psychosis in children with velocardiofacial syndrome (22q11.2 deletion syndrome) |
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