Literature DB >> 23810929

An analysis of the topography, severity, potential sources of reinforcement, and treatments utilized for skin picking in Prader-Willi syndrome.

Kristin M Hustyi1, Jennifer L Hammond, Ava B Rezvani, Scott S Hall.   

Abstract

We examined the topography, severity, potential sources of reinforcement, and treatments utilized for skin-picking behavior shown by individuals with Prader-Willi syndrome (PWS). The parents of 55 individuals with PWS, aged 6-25 years, were interviewed about their child's skin-picking behavior using the Self-Injury Trauma Scale (SIT; Iwata, Pace, Kissel, Nau, & Farber, 1990) and the Functional Analysis Screening Tool (FAST; Iwata, DeLeon, & Roscoe, 2013). Results showed that skin picking in PWS occurred on the extremities (i.e., arms, legs, hands, and feet) for 75% of cases and resulted in bodily injury for 83.7% cases. Skin picking posed a high risk to the individual concerned in 41.8% of cases. Automatic sensory stimulation was identified as a potential source of reinforcement in the majority of cases (52.7%) followed by access to social attention or preferred items (36.4%). Treatments utilized by parents were primarily behavioral strategies (56.3%) followed by basic first aid (54.5%). There were no differences in the topography, severity or potential source of reinforcement between those with the deletion (DEL) subtype and those with the uniparental disomy (UPD) subtype. Taken together, these data indicate that skin picking shown by individuals with PWS is a particularly severe and intractable behavioral issue that may be maintained by (as yet unknown) sensory consequences. Further studies to identify the determinants of skin picking in PWS are therefore needed. The implications for interventions are discussed.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Automatic reinforcement; Functional assessment; Prader–Willi syndrome; Self-injurious behavior; Skin picking

Mesh:

Year:  2013        PMID: 23810929     DOI: 10.1016/j.ridd.2013.06.014

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


  9 in total

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2.  Neural correlates of self-injurious behavior in Prader-Willi syndrome.

Authors:  Megan Klabunde; Manish Saggar; Kristin M Hustyi; Jennifer L Hammond; Allan L Reiss; Scott S Hall
Journal:  Hum Brain Mapp       Date:  2015-07-14       Impact factor: 5.038

3.  Skin Picking in People with Prader-Willi Syndrome: Phenomenology and Management.

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4.  Problem behaviour in adolescent boys with fragile X syndrome: relative prevalence, frequency and severity.

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Review 5.  Behavioral treatment of automatically reinforced SIB: 1982 - 2015.

Authors:  Griffin W Rooker; Andrew C Bonner; Christopher M Dillon; Jennifer R Zarcone
Journal:  J Appl Behav Anal       Date:  2018-07-10

6.  Brief Report: Challenging Behaviors in Toddlers and Preschoolers with Angelman, Prader-Willi, and Williams Syndromes.

Authors:  Wei Siong Neo; Bridgette L Tonnsen
Journal:  J Autism Dev Disord       Date:  2019-04

7.  Prolapsed Rectum and Risk Factors in Prader-Willi Syndrome: A Case-Based Review.

Authors:  Merlin G Butler
Journal:  J Pediatr Genet       Date:  2021-03-03

8.  Anomalous basal ganglia connectivity and obsessive-compulsive behaviour in patients with Prader Willi syndrome.

Authors:  Jesus Pujol; Laura Blanco-Hinojo; Susanna Esteba-Castillo; Assumpta Caixàs; Ben J Harrison; Marta Bueno; Joan Deus; Mercedes Rigla; Dídac Macià; Jone Llorente-Onaindia; Ramón Novell-Alsina
Journal:  J Psychiatry Neurosci       Date:  2016-06       Impact factor: 6.186

Review 9.  The RDoC approach for translational psychiatry: Could a genetic disorder with psychiatric symptoms help fill the matrix? the example of Prader-Willi syndrome.

Authors:  Juliette Salles; Emmanuelle Lacassagne; Grégoire Benvegnu; Sophie Çabal Berthoumieu; Nicolas Franchitto; Maithé Tauber
Journal:  Transl Psychiatry       Date:  2020-08-08       Impact factor: 6.222

  9 in total

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