Literature DB >> 24594523

The prevalence of aggression in genetic syndromes: a review.

Laurie Powis1, Chris Oliver2.   

Abstract

Research into behavioural phenotypes identifies both environmental and organic factors as influencing aggression in children and adults with genetic disorders associated with intellectual disability. However, in contrast to self-injury there is a paucity of research that compares aggression across relevant syndromes. The primary aim of this review is to examine the association between aggression and genetic syndromes by analysis of prevalence studies. The review also examines the literature on the form of the behaviour and influence of environmental factors. Results imply that certain syndrome groups (Cri du Chat, Smith-Magenis, Prader-Willi, Angelman, Cornelia de Lange, and Fragile X syndromes; estimates over 70%) evidence a stronger association with aggression than others (e.g. Williams and Down syndromes; estimates below 15%). However, the strength of association is difficult to quantify due to methodological differences between studies. The results from examining form and environmental influences highlight the importance of phenotype-environment interactions. Research employing group comparison designs is warranted and future work on the assessment and intervention of aggression in genetic syndromes should consider the importance of phenotype-environment interactions.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Aggression; Behavioural phenotype; Genetic syndrome; Intellectual disability; Prevalence

Mesh:

Year:  2014        PMID: 24594523     DOI: 10.1016/j.ridd.2014.01.033

Source DB:  PubMed          Journal:  Res Dev Disabil        ISSN: 0891-4222


  8 in total

1.  Longitudinal trajectories of aberrant behavior in fragile X syndrome.

Authors:  Kristin M Hustyi; Scott S Hall; Booil Jo; Amy A Lightbody; Allan L Reiss
Journal:  Res Dev Disabil       Date:  2014-08-15

Review 2.  Developmental trajectories in 22q11.2 deletion.

Authors:  Ann Swillen; Donna McDonald-McGinn
Journal:  Am J Med Genet C Semin Med Genet       Date:  2015-05-18       Impact factor: 3.908

3.  Development, behavior, and biomarker characterization of Smith-Lemli-Opitz syndrome: an update.

Authors:  Audrey Thurm; Elaine Tierney; Cristan Farmer; Phebe Albert; Lisa Joseph; Susan Swedo; Simona Bianconi; Irena Bukelis; Courtney Wheeler; Geeta Sarphare; Diane Lanham; Christopher A Wassif; Forbes D Porter
Journal:  J Neurodev Disord       Date:  2016-04-05       Impact factor: 4.025

4.  Caregiver Training in Mindfulness-Based Positive Behavior Supports (MBPBS): Effects on Caregivers and Adults with Intellectual and Developmental Disabilities.

Authors:  Nirbhay N Singh; Giulio E Lancioni; Bryan T Karazsia; Rachel E Myers
Journal:  Front Psychol       Date:  2016-02-09

Review 5.  Unmet clinical needs and burden in Angelman syndrome: a review of the literature.

Authors:  Anne C Wheeler; Patricia Sacco; Raquel Cabo
Journal:  Orphanet J Rare Dis       Date:  2017-10-16       Impact factor: 4.123

6.  An 18-year-old patient with Prader-Willi syndrome: a case report on dental management under sedation and general anesthesia.

Authors:  Ki Un Song; Ok Hyung Nam; Mi Sun Kim; Sung Chul Choi; Hyo-Seol Lee
Journal:  J Dent Anesth Pain Med       Date:  2015-12-31

7.  Intrafamily and intragenomic conflicts in human warfare.

Authors:  Alberto J C Micheletti; Graeme D Ruxton; Andy Gardner
Journal:  Proc Biol Sci       Date:  2017-02-22       Impact factor: 5.349

8.  Behavioral disorder in people with an intellectual disability and epilepsy: A report of the Intellectual Disability Task Force of the Neuropsychiatric Commission of ILAE.

Authors:  Mike Kerr; Christine Linehan; Christian Brandt; Kousuke Kanemoto; Jun Kawasaki; Kenji Sugai; Yukari Tadokoro; Vicente Villanueva; Jo Wilmshurst; Sarah Wilson
Journal:  Epilepsia Open       Date:  2016-09-15
  8 in total

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