Literature DB >> 28806899

Executive functioning in Cornelia de Lange syndrome: domain asynchrony and age-related performance.

Donna Reid1, Jo Moss2,3, Lisa Nelson1, Laura Groves1, Chris Oliver1.   

Abstract

BACKGROUND: The aim of this study was to examine executive functioning in adolescents and adults with Cornelia de Lange syndrome (CdLS) to identify a syndrome and age-related profile of cognitive impairment.
METHODS: Participants were 24 individuals with CdLS aged 13-42 years (M = 22; SD = 8.98), and a comparable contrast group of 21 individuals with Down syndrome (DS) aged 15-33 years (M = 24; SD = 5.82). Measures were selected to test verbal and visual fluency, inhibition, perseverance/flexibility, and working memory and comprised both questionnaire and performance tests.
RESULTS: Individuals with CdLS showed significantly greater impairment on tasks requiring flexibility and inhibition (rule switch) and on forwards span capacity. These impairments were also reported in the parent/carer-rated questionnaire measures. Backwards Digit Span was significantly negatively correlated with chronological age in CdLS, indicating increased deficits with age. This was not identified in individuals with DS.
CONCLUSIONS: The relative deficits in executive functioning task performance are important in understanding the behavioural phenotype of CdLS. Prospective longitudinal follow-up is required to examine further the changes in executive functioning with age and if these map onto observed changes in behaviour in CdLS. Links with recent research indicating heightened responses to oxidative stress in CdLS may also be important.

Entities:  

Keywords:  Behavioural phenotype; CdLS; Cornelia de Lange; Executive functioning

Year:  2017        PMID: 28806899      PMCID: PMC5556702          DOI: 10.1186/s11689-017-9208-7

Source DB:  PubMed          Journal:  J Neurodev Disord        ISSN: 1866-1947            Impact factor:   4.025


  59 in total

1.  Executive functions among youth with Down Syndrome and co-existing neurobehavioural disorders.

Authors:  A E Pritchard; S Kalback; M McCurdy; G T Capone
Journal:  J Intellect Disabil Res       Date:  2015-09-15

2.  de Lange syndrome: a clinical review of 310 individuals.

Authors:  L Jackson; A D Kline; M A Barr; S Koch
Journal:  Am J Med Genet       Date:  1993-11-15

3.  RAD21 mutations cause a human cohesinopathy.

Authors:  Matthew A Deardorff; Jonathan J Wilde; Melanie Albrecht; Emma Dickinson; Stephanie Tennstedt; Diana Braunholz; Maren Mönnich; Yuqian Yan; Weizhen Xu; María Concepcion Gil-Rodríguez; Dinah Clark; Hakon Hakonarson; Sara Halbach; Laura Daniela Michelis; Abhinav Rampuria; Eva Rossier; Stephanie Spranger; Lionel Van Maldergem; Sally Ann Lynch; Gabriele Gillessen-Kaesbach; Hermann-Josef Lüdecke; Robert G Ramsay; Michael J McKay; Ian D Krantz; Huiling Xu; Julia A Horsfield; Frank J Kaiser
Journal:  Am J Hum Genet       Date:  2012-05-24       Impact factor: 11.025

4.  X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations.

Authors:  Antonio Musio; Angelo Selicorni; Maria Luisa Focarelli; Cristina Gervasini; Donatella Milani; Silvia Russo; Paolo Vezzoni; Lidia Larizza
Journal:  Nat Genet       Date:  2006-04-09       Impact factor: 38.330

5.  The effects of experience on attribution of a stereotyped personality to children with Down's syndrome.

Authors:  J G Wishart; F H Johnston
Journal:  J Ment Defic Res       Date:  1990-10

6.  Survey of speech and language skills with prognostic indicators in 116 patients with Cornelia de Lange syndrome.

Authors:  M T Goodban
Journal:  Am J Med Genet       Date:  1993-11-15

7.  Neuropathological analysis of an adult case of the Cornelia de Lange syndrome.

Authors:  Nicolas Vuilleumier; Enikö Kövari; Agnès Michon; Patrick R Hof; Georges Mentenopoulos; Panteleimon Giannakopoulos; Constantin Bouras
Journal:  Acta Neuropathol       Date:  2002-05-30       Impact factor: 17.088

8.  Cognitive executive function in Down's syndrome.

Authors:  John Rowe; Anthony Lavender; Vicky Turk
Journal:  Br J Clin Psychol       Date:  2006-03

9.  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

10.  A specific pathway can be identified between genetic characteristics and behaviour profiles in Prader-Willi syndrome via cognitive, environmental and physiological mechanisms.

Authors:  K A Woodcock; C Oliver; G W Humphreys
Journal:  J Intellect Disabil Res       Date:  2009-06
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  9 in total

1.  A Behavioural Assessment of Social Anxiety and Social Motivation in Fragile X, Cornelia de Lange and Rubinstein-Taybi Syndromes.

Authors:  Hayley Crawford; Joanna Moss; Laura Groves; Robyn Dowlen; Lisa Nelson; Donna Reid; Chris Oliver
Journal:  J Autism Dev Disord       Date:  2020-01

2.  Development, behaviour and sensory processing in Marshall-Smith syndrome and Malan syndrome: phenotype comparison in two related syndromes.

Authors:  P A Mulder; I D C van Balkom; A M Landlust; M Priolo; L A Menke; I H Acero; F S Alkuraya; P Arias; L Bernardini; E K Bijlsma; T Cole; C Coubes; I Dapia; S Davies; N Di Donato; N H Elcioglu; J A Fahrner; A Foster; N G González; I Huber; M Iascone; A-S Kaiser; A Kamath; K Kooblall; P Lapunzina; J Liebelt; S A Lynch; S M Maas; C Mammì; I B Mathijssen; S McKee; G M Mirzaa; T Montgomery; D Neubauer; T E Neumann; L Pintomalli; M A Pisanti; A S Plomp; S Price; C Salter; F Santos-Simarro; P Sarda; D Schanze; M Segovia; C Shaw-Smith; S Smithson; M Suri; K Tatton-Brown; J Tenorio; R V Thakker; R M Valdez; A Van Haeringen; J M Van Hagen; M Zenker; M Zollino; W W Dunn; S Piening; R C Hennekam
Journal:  J Intellect Disabil Res       Date:  2020-10-09

3.  Cornelia De Lange Syndrome In A 4-Year-Old Child From India: Phenotype Description And Role Of Genetic Counseling.

Authors:  Girish Gulab Meshram; Neeraj Kaur; Kanwaljeet Singh Hura
Journal:  Med Arch       Date:  2018-10

4.  Lifespan trajectory of affect in Cornelia de Lange syndrome: towards a neurobiological hypothesis.

Authors:  Laura Groves; Joanna Moss; Hayley Crawford; Lisa Nelson; Chris Stinton; Gursharan Singla; Chris Oliver
Journal:  J Neurodev Disord       Date:  2019-06-07       Impact factor: 4.025

5.  Age-related Behavioural Change in Cornelia de Lange and Cri du Chat Syndromes: A Seven Year Follow-up Study.

Authors:  Lisa Cochran; Alice Welham; Chris Oliver; Adam Arshad; Joanna F Moss
Journal:  J Autism Dev Disord       Date:  2019-06

6.  Divergent presentation of anxiety in high-risk groups within the intellectual disability population.

Authors:  Laura Groves; Joanna Moss; Chris Oliver; Rachel Royston; Jane Waite; Hayley Crawford
Journal:  J Neurodev Disord       Date:  2022-10-05       Impact factor: 4.074

Review 7.  Memory profiles in Down syndrome across development: a review of memory abilities through the lifespan.

Authors:  Mary Godfrey; Nancy Raitano Lee
Journal:  J Neurodev Disord       Date:  2018-01-29       Impact factor: 4.025

Review 8.  Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement.

Authors:  Antonie D Kline; Joanna F Moss; Angelo Selicorni; Anne-Marie Bisgaard; Matthew A Deardorff; Peter M Gillett; Stacey L Ishman; Lynne M Kerr; Alex V Levin; Paul A Mulder; Feliciano J Ramos; Jolanta Wierzba; Paola Francesca Ajmone; David Axtell; Natalie Blagowidow; Anna Cereda; Antonella Costantino; Valerie Cormier-Daire; David FitzPatrick; Marco Grados; Laura Groves; Whitney Guthrie; Sylvia Huisman; Frank J Kaiser; Gerritjan Koekkoek; Mary Levis; Milena Mariani; Joseph P McCleery; Leonie A Menke; Amy Metrena; Julia O'Connor; Chris Oliver; Juan Pie; Sigrid Piening; Carol J Potter; Ana L Quaglio; Egbert Redeker; David Richman; Claudia Rigamonti; Angell Shi; Zeynep Tümer; Ingrid D C Van Balkom; Raoul C Hennekam
Journal:  Nat Rev Genet       Date:  2018-10       Impact factor: 53.242

9.  An Observational Study of Social Interaction Skills and Behaviors in Cornelia de Lange, Fragile X and Rubinstein-Taybi Syndromes.

Authors:  Katherine Ellis; Chris Oliver; Chrysi Stefanidou; Ian Apperly; Jo Moss
Journal:  J Autism Dev Disord       Date:  2020-11
  9 in total

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