The behavioural phenotype of Potocki-Lupski syndrome: a cross-syndrome comparison

被引:14
作者
Bissell, Stacey [1 ]
Wilde, Lucy [1 ]
Richards, Caroline [1 ]
Moss, Jo [1 ,2 ]
Oliver, Chris [1 ]
机构
[1] Univ Birmingham, Sch Psychol, Cerebra Ctr Neurodev Disorders, Birmingham B15 2TT, W Midlands, England
[2] UCL, Inst Cognit Neurosci, Alexandra House,17-19 Queen Sq, London WC1N 3AR, England
关键词
Autism spectrum disorder; Behavioural phenotype; Challenging behaviour; Impulsivity; Potocki-Lupski syndrome; Repetitive behaviour; Self-injury; Smith-Magenis syndrome; SMITH-MAGENIS-SYNDROME; AUTISM SPECTRUM DISORDERS; SYNDROME DEL 17P11.2; HOMOLOGOUS RECOMBINATION; DUPLICATION; 17P11.2; INTELLECTUAL DISABILITY; GENETIC SYNDROMES; ANGELMAN-SYNDROME; PRADER-WILLI; RAI1;
D O I
10.1186/s11689-017-9221-x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Potocki-Lupski syndrome (PTLS) and Smith-Magenis syndrome (SMS) are related genomic disorders, as duplication 17p11.2 (associated with PTLS) is the reciprocal recombination product of the SMS microdeletion. While SMS has a relatively well-delineated behavioural phenotype, the behavioural profile in PTLS is less well defined, despite purported associations with autism spectrum disorder (ASD) and the suggestion that some behaviours may be diametric to those seen in SMS. Methods: Caregivers of individuals with PTLS (N = 34; M age = 12.43, SD = 6.78) completed online behavioural questionnaires, including the Challenging Behaviour Questionnaire (CBQ), the Activity Questionnaire (TAQ), the Repetitive Behaviour Questionnaire (RBQ), the Mood, Interest and Pleasure Questionnaire-Short Form (MIPQ-S) and the Social Communication Questionnaire (SCQ), which assesses behaviours associated with ASD. Individuals with PTLS were matched on age and adaptive functioning to individuals with SMS (N = 31; M age = 13.61, SD = 6.85) and individuals with idiopathic ASD (N = 33; M age = 12.04, SD = 5.85) from an existing dataset. Results: Individuals with PTLS and SMS were less impaired than those with idiopathic ASD on the communication and reciprocal social interaction subscales of the SCQ, but neither syndrome group differed from idiopathic ASD on the restricted, repetitive and stereotyped behaviours subscale. On the repetitive behaviour measure, individuals with PTLS and idiopathic ASD scored higher than individuals with SMS on the compulsive behaviour subscale. Rates of self-injury and property destruction were significantly lower in PTLS and idiopathic ASD than in SMS. No between-syndrome differences were found in relation to overactivity or mood; however, impulsivity was greater in SMS than in PTLS. Conclusions: Findings suggest some overlap in the behavioural phenotype of PTLS and features of ASD symptomatology; however, the overall profile of behaviours in PTLS appears to be divergent from both idiopathic ASD and SMS. Relative to idiopathic ASD, PTLS is not characterised by communication or social interaction deficits. However, restricted and repetitive behaviours were evident in PTLS, and these may be characterised specifically by compulsive behaviours. While several behavioural differences were identified between PTLS and SMS, there was little evidence of diametric behavioural phenotypes, particularly in relation to social behaviour.
引用
收藏
页数:9
相关论文
共 71 条
[1]   The prevalence and phenomenology of self-injurious and aggressive behaviour in genetic syndromes [J].
Arron, K. ;
Oliver, C. ;
Moss, J. ;
Berg, K. ;
Burbidge, C. .
JOURNAL OF INTELLECTUAL DISABILITY RESEARCH, 2011, 55 :109-120
[2]   Autism screening questionnaire: diagnostic validity [J].
Berument, SK ;
Rutter, M ;
Lord, C ;
Pickles, A ;
Bailey, A .
BRITISH JOURNAL OF PSYCHIATRY, 1999, 175 :444-451
[3]   Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes [J].
Bi, Weimin ;
Yan, Jiong ;
Shi, Xin ;
Yuva-Paylor, Lisa A. ;
Antalffy, Barbara A. ;
Goldman, Alica ;
Yoo, Jong W. ;
Noebels, Jeffrey L. ;
Armstrong, Dawna L. ;
Paylor, Richard ;
Lupski, James R. .
HUMAN MOLECULAR GENETICS, 2007, 16 (15) :1802-1813
[4]   Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome [J].
Bi, WM ;
Saifi, GM ;
Shaw, CJ ;
Walz, K ;
Fonseca, P ;
Wilson, M ;
Potocki, L ;
Lupski, JR .
HUMAN GENETICS, 2004, 115 (06) :515-524
[5]   Mental health and intellectual disability: III [J].
Bouras, N .
JOURNAL OF INTELLECTUAL DISABILITY RESEARCH, 1998, 42 :439-439
[6]   The association between repetitive behaviours, impulsivity and hyperactivity in people with intellectual disability [J].
Burbidge, C. ;
Oliver, C. ;
Moss, J. ;
Arron, K. ;
Berg, K. ;
Furniss, F. ;
Hill, L. ;
Trusler, K. ;
Woodock, K. .
JOURNAL OF INTELLECTUAL DISABILITY RESEARCH, 2010, 54 :1078-1092
[7]  
Burbidge C., 2008, The Activity Questionnaire. Manual for administration and score interpretation
[8]  
Cassidy SB, 2000, AM J MED GENET, V97, P136, DOI 10.1002/1096-8628(200022)97:2<136::AID-AJMG5>3.0.CO
[9]  
2-V
[10]   Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome [J].
Chen, KS ;
Manian, P ;
Koeuth, T ;
Potocki, L ;
Zhao, Q ;
Chinault, AC ;
Lee, CC ;
Lupski, JR .
NATURE GENETICS, 1997, 17 (02) :154-163