Literature DB >> 9833657

Problem behaviors associated with deletion Prader-Willi, Smith-Magenis, and cri du chat syndromes.

D J Clarke1, H Boer.   

Abstract

Problem behaviors of individuals who had one of three chromosome deletion disorders (5p- cri-du-chat, 15q- Prader-Willi, or 17p- Smith-Magenis) were investigated. The Aberrant Behavior Checklist was used. Results were contrasted with those of two groups of people with mental retardation who were described in other studies. The checklist rates many, but not all, potentially relevant behaviors. Eating abnormalities, known to be problematic in Prader-Willi syndrome, and sleep abnormalities, believed to be problematic in Smith-Magenis syndrome, were not included in the survey. All three disorders were associated with greater ratings of problem behaviors than the comparison groups on at least one subscale of the checklist. The results lend support to the partial specificity model of behaviors associated with genetically determined syndromes.

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Year:  1998        PMID: 9833657     DOI: 10.1352/0895-8017(1998)103<0264:PBAWDP>2.0.CO;2

Source DB:  PubMed          Journal:  Am J Ment Retard        ISSN: 0895-8017


  12 in total

1.  An indirect examination of the function of problem behavior associated with fragile X syndrome and Smith-Magenis syndrome.

Authors:  Paul Langthorne; Peter McGill
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2.  Adaptive and maladaptive behavior in children with Smith-Magenis Syndrome.

Authors:  Staci C Martin; Pamela L Wolters; Ann C M Smith
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3.  Factor analysis of the aberrant behavior checklist in individuals with autism spectrum disorders.

Authors:  Jason Brinkley; Laura Nations; Ruth K Abramson; Alicia Hall; Harry H Wright; Robin Gabriels; John R Gilbert; Margaret A O Pericak-Vance; Michael L Cuccaro
Journal:  J Autism Dev Disord       Date:  2006-12-21

4.  Genetic subtype differences in neural circuitry of food motivation in Prader-Willi syndrome.

Authors:  L M Holsen; J R Zarcone; R Chambers; M G Butler; D C Bittel; W M Brooks; T I Thompson; C R Savage
Journal:  Int J Obes (Lond)       Date:  2008-12-02       Impact factor: 5.095

5.  Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome.

Authors:  Paulina Carmona-Mora; Carolina A Encina; Cesar P Canales; Lei Cao; Jessica Molina; Pamela Kairath; Juan I Young; Katherina Walz
Journal:  BMC Mol Biol       Date:  2010-08-25       Impact factor: 2.946

6.  The prevalence and phenomenology of repetitive behavior in genetic syndromes.

Authors:  Joanna Moss; Chris Oliver; Kate Arron; Cheryl Burbidge; Katy Berg
Journal:  J Autism Dev Disord       Date:  2008-11-27

7.  Schizophrenia and birthplace of paternal and maternal grandfather in the Jerusalem perinatal cohort prospective study.

Authors:  S Harlap; M C Perrin; L Deutsch; K Kleinhaus; S Fennig; D Nahon; A Teitelbaum; Y Friedlander; D Malaspina
Journal:  Schizophr Res       Date:  2009-04-09       Impact factor: 4.939

8.  The pathophysiology of restricted repetitive behavior.

Authors:  Mark Lewis; Soo-Jeong Kim
Journal:  J Neurodev Disord       Date:  2009-06-16       Impact factor: 4.025

Review 9.  Cri du Chat syndrome.

Authors:  Paola Cerruti Mainardi
Journal:  Orphanet J Rare Dis       Date:  2006-09-05       Impact factor: 4.123

10.  Mouse models of genomic syndromes as tools for understanding the basis of complex traits: an example with the smith-magenis and the potocki-lupski syndromes.

Authors:  P Carmona-Mora; J Molina; C A Encina; K Walz
Journal:  Curr Genomics       Date:  2009-06       Impact factor: 2.236

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