Literature DB >> 21743818

Discordance in Diagnoses and Treatment of Psychiatric Disorders in Children and Adolescents with 22q11.2 Deletion Syndrome.

Andrea S Young1, Vandana Shashi, Kelly Schoch, Thomas Kwapil, Stephen R Hooper.   

Abstract

This study examines the rate of utilization of mental health services in children and adolescents with 22q11DS relative to their remarkably high rate of psychiatric disorders and behavior problems. Seventy-two children and adolescents with 22q11DS were participants; their parents completed the Diagnostic Interview Schedule for Children (DISC) and the Child Behavior Checklist (CBCL). The results indicated that 22q11DS children and adolescents have higher rates of psychopathology than the general pediatric population, with ADHD and anxiety disorders being the most common. However, among youth with 22q11DS, those with psychopathology are often no more likely to receive either pharmacological or non-pharmacological mental health care than those without a given psychiatric diagnosis. Thus, although psychopathology is fairly common in this sample, many children with 22q11DS may not be receiving needed psychiatric care. These results have significant implications for these children and their families, as well as for the health care providers who treat them. In particular, the results may suggest a need for careful screening of psychiatric disorders that are likely to affect this population as well, as making appropriate treatment recommendations to remedy childhood mental health problems. Since these children face an extraordinarily high risk of psychoses in late adolescence/adulthood, treatment of childhood psychopathology could be crucial in mitigating the risk/consequences of major psychiatric illnesses in later life.

Entities:  

Year:  2011        PMID: 21743818      PMCID: PMC3129857          DOI: 10.1016/j.ajp.2011.03.002

Source DB:  PubMed          Journal:  Asian J Psychiatr        ISSN: 1876-2018


  42 in total

1.  A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

Authors:  D A Driscoll; M L Budarf; B S Emanuel
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

2.  COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome.

Authors:  Vandana Shashi; Timothy D Howard; Matcheri S Keshavan; Jessica Kaczorowski; Margaret N Berry; Kelly Schoch; Edward J Spence; Thomas R Kwapil
Journal:  Psychiatry Res       Date:  2010-05-20       Impact factor: 3.222

3.  Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study.

Authors:  Linda E Campbell; Eileen Daly; Fiona Toal; Angela Stevens; Rayna Azuma; Marco Catani; Virginia Ng; Therese van Amelsvoort; Xavier Chitnis; William Cutter; Declan G M Murphy; Kieran C Murphy
Journal:  Brain       Date:  2006-03-28       Impact factor: 13.501

4.  Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives.

Authors:  A E Pulver; G Nestadt; R Goldberg; R J Shprintzen; M Lamacz; P S Wolyniec; B Morrow; M Karayiorgou; S E Antonarakis; D Housman
Journal:  J Nerv Ment Dis       Date:  1994-08       Impact factor: 2.254

5.  Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome.

Authors:  Kathryn Eve Lewandowski; Vandana Shashi; Peggy M Berry; Thomas R Kwapil
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2007-01-05       Impact factor: 3.568

6.  Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

Authors:  D F Papolos; G L Faedda; S Veit; R Goldberg; B Morrow; R Kucherlapati; R J Shprintzen
Journal:  Am J Psychiatry       Date:  1996-12       Impact factor: 18.112

7.  The Great Smoky Mountains Study of Youth. Goals, design, methods, and the prevalence of DSM-III-R disorders.

Authors:  E J Costello; A Angold; B J Burns; D K Stangl; D L Tweed; A Erkanli; C M Worthman
Journal:  Arch Gen Psychiatry       Date:  1996-12

Review 8.  Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes.

Authors:  Lisa J Kobrynski; Kathleen E Sullivan
Journal:  Lancet       Date:  2007-10-20       Impact factor: 79.321

9.  Living with a child at risk for psychotic illness: the experience of parents coping with 22q11 deletion syndrome: an exploratory study.

Authors:  Laura Hercher; Georgette Bruenner
Journal:  Am J Med Genet A       Date:  2008-09-15       Impact factor: 2.802

Review 10.  Velo-cardio-facial syndrome: 30 Years of study.

Authors:  Robert J Shprintzen
Journal:  Dev Disabil Res Rev       Date:  2008
View more
  16 in total

1.  Social cognitive training in adolescents with chromosome 22q11.2 deletion syndrome: feasibility and preliminary effects of the intervention.

Authors:  V Shashi; W Harrell; S Eack; C Sanders; A McConkie-Rosell; M S Keshavan; M J Bonner; K Schoch; S R Hooper
Journal:  J Intellect Disabil Res       Date:  2015-04-14

2.  Disclosure of psychiatric manifestations of 22q11.2 deletion syndrome in medical genetics: A 12-year retrospective chart review.

Authors:  Serena Talcott Baughman; Emily Morris; Kimberly Jensen; Jehannine Austin
Journal:  Am J Med Genet A       Date:  2015-05-31       Impact factor: 2.802

3.  Non-pharmacological treatment of psychiatric disorders in individuals with 22q11.2 deletion syndrome; a systematic review.

Authors:  Petra C M Buijs; Anne S Bassett; Erik Boot
Journal:  Am J Med Genet A       Date:  2018-01-24       Impact factor: 2.802

4.  A Genomically Informed Education System? Challenges for Behavioral Genetics.

Authors:  Maya Sabatello
Journal:  J Law Med Ethics       Date:  2018-03-27       Impact factor: 1.718

5.  Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome.

Authors:  T M Allen; J Hersh; K Schoch; K Curtiss; S R Hooper; V Shashi
Journal:  J Intellect Disabil Res       Date:  2013-06-07

6.  Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms.

Authors:  Vandana Shashi; Alan Francis; Stephen R Hooper; Peter G Kranz; Michael Zapadka; Kelly Schoch; Edward Ip; Neeraj Tandon; Timothy D Howard; Matcheri S Keshavan
Journal:  Eur J Hum Genet       Date:  2012-06-27       Impact factor: 4.246

Review 7.  Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.

Authors:  N Hiroi; T Takahashi; A Hishimoto; T Izumi; S Boku; T Hiramoto
Journal:  Mol Psychiatry       Date:  2013-08-06       Impact factor: 15.992

8.  Axis I psychiatric diagnoses in adolescents and young adults with 22q11 deletion syndrome.

Authors:  O Y Ousley; E Smearman; S Fernandez-Carriba; K A Rockers; K Coleman; E F Walker; J F Cubells
Journal:  Eur Psychiatry       Date:  2013-08-02       Impact factor: 5.361

9.  A longitudinal examination of the psychoeducational, neurocognitive, and psychiatric functioning in children with 22q11.2 deletion syndrome.

Authors:  Stephen R Hooper; Kathleen Curtiss; Kelly Schoch; Matcheri S Keshavan; Andrew Allen; Vandana Shashi
Journal:  Res Dev Disabil       Date:  2013-03-16

10.  An examination of the relationship of anxiety and intelligence to adaptive functioning in children with chromosome 22q11.2 deletion syndrome.

Authors:  Kathleen Angkustsiri; Ingrid Leckliter; Nicole Tartaglia; Elliott A Beaton; Janice Enriquez; Tony J Simon
Journal:  J Dev Behav Pediatr       Date:  2012 Nov-Dec       Impact factor: 2.225

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.