Core neuropsychological characteristics of children and adolescents with 22q11.2 deletion

被引:35
|
作者
Jacobson, C. [1 ]
Shearer, J. [3 ]
Habel, A. [2 ]
Kane, F. [1 ]
Tsakanikos, E. [1 ]
Kravariti, E. [1 ]
机构
[1] Kings Coll London, Kings Hlth Partners, Inst Psychiat, Dept Psychosis Studies, London SE5 8AF, England
[2] Great Ormond St Hosp Sick Children, N Thames Cleft Lip Palate Serv, London WC1N 3JH, England
[3] Great Ormond St Hosp Sick Children, Psychosocial & Family Serv, London WC1N 3JH, England
关键词
22q11; 2; deletion; adolescent; child; intellectual disability; neuropsychology; CARDIO-FACIAL-SYNDROME; VELOCARDIOFACIAL SYNDROME; NEUROCOGNITIVE PHENOTYPE; SPECTRUM DISORDERS; SYNDROME VCFS; YOUNG-ADULTS; SCHIZOPHRENIA; PROFILE; ATTENTION; LANGUAGE;
D O I
10.1111/j.1365-2788.2010.01298.x
中图分类号
G76 [特殊教育];
学科分类号
040109 ;
摘要
Background The 22q11.2 deletion syndrome (22qDS) confers high risk for intellectual disability and neuropsychological/academic impairment, although a minority of patients show average intelligence. Intellectual heterogeneity and the high prevalence of psychiatric diagnoses in earlier studies may have obscured the prototypical neuropsychological profile in 22qDS. Methods We examined intelligence, memory, reading and mathematical processes in 31 children/adolescents with 22qDS, selected for educational underachievement and an absence of psychiatric diagnoses, using standardised, psychometrically matched instruments that specify how typical a score is for a given intelligence quotient (IQ). Results Corroborating earlier findings, verbal IQ was significantly superior to performance IQ; verbal memory and basic reading were relative strengths; and visual/spatial memory was a relative weakness. All four findings transcended performance characteristics that are typical of low-IQ individuals. Rote learning yielded the highest score; reading comprehension, numerical operations and mathematical reasoning were among the lowest-performed academic domains. Albeit in the expected direction, performance in the respective components could not be clearly differentiated from what is IQ-appropriate. Conclusions A superiority of verbal intelligence over non-verbal intelligence, relative strengths in verbal memory and basic reading, and a relative weakness in visual/spatial memory are likely to be core characteristics of children/adolescents with 22qDS, transcending performance features that are typical of individuals with low IQ.
引用
收藏
页码:701 / 713
页数:13
相关论文
共 50 条
  • [1] Visuomotor abilities and neuropsychological functioning in children and adolescents with 22q11.2 Deletion Syndrome
    Howley, S.
    Prasad, S. E.
    Pender, N. P.
    Murphy, K. C.
    JOURNAL OF INTELLECTUAL DISABILITY RESEARCH, 2007, 51 : 655 - 655
  • [2] Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion
    Woodin, M
    Wang, PP
    Aleman, D
    McDonald-McGinn, D
    Zackai, E
    Moss, E
    GENETICS IN MEDICINE, 2001, 3 (01) : 34 - 39
  • [3] Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome:: Neuropsychological and behavioral implications
    Debbané, M
    Glaser, B
    David, MK
    Feinstein, C
    Eliez, S
    SCHIZOPHRENIA RESEARCH, 2006, 84 (2-3) : 187 - 193
  • [4] Neuropsychological Profile of Italian Children and Adolescents with 22q11.2 Deletion Syndrome with and Without Intellectual Disability
    Vicari, Stefano
    Mantovan, Manuela
    Addona, Francesca
    Costanzo, Floriana
    Verucci, Lorena
    Menghini, Deny
    BEHAVIOR GENETICS, 2012, 42 (02) : 287 - 298
  • [5] Neuropsychological Profile of Italian Children and Adolescents with 22q11.2 Deletion Syndrome with and Without Intellectual Disability
    Stefano Vicari
    Manuela Mantovan
    Francesca Addona
    Floriana Costanzo
    Lorena Verucci
    Deny Menghini
    Behavior Genetics, 2012, 42 : 287 - 298
  • [6] Neuropsychological profile of adolescent with 22q11.2 Deletion Syndrome
    Smith, M.
    Masur, D.
    Mcginley, J.
    Weiss, E.
    Fachinni, R.
    ARCHIVES OF CLINICAL NEUROPSYCHOLOGY, 2020, 35 (06) : 985 - 985
  • [7] Tonsillectomy in Children with 22q11.2 Deletion Syndrome
    Arganbright, Jill M.
    Hankey, Paul Bryan
    Tracy, Meghan
    Narayanan, Srivats
    Noel-MacDonnell, Janelle
    Ingram, David
    GENES, 2022, 13 (12)
  • [8] Autism in children with 22Q11.2 deletion syndrome
    Eliez, Stephan
    JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 2007, 46 (04): : 433 - 434
  • [9] Atypical neuropsychological profile in a boy with 22q11.2 Deletion Syndrome
    Stiers, P
    Swillen, A
    De Smedt, B
    Lagae, L
    Devriendt, K
    D'Agostino, E
    Sunaert, S
    Fryns, JP
    CHILD NEUROPSYCHOLOGY, 2005, 11 (01) : 87 - 108
  • [10] Schizotypal traits in adolescents with 22q11.2 deletion syndrome
    Fonseca-Pedrero, Eduardo
    Debbane, Martin
    Schneider, Maude
    Badoud, Deborah
    Ortuno-Sierra, Javier
    Eliez, Stephan
    EUROPEAN CHILD & ADOLESCENT PSYCHIATRY, 2015, 24 : S77 - S77