Literature DB >> 25989416

Contrasting age related changes in autism spectrum disorder phenomenology in Cornelia de Lange, Fragile X, and Cri du Chat syndromes: Results from a 2.5 year follow-up.

Lisa Cochran, Joanna Moss, Lisa Nelson, Chris Oliver.   

Abstract

Little is known about the way in which the characteristics of autism spectrum disorder (ASD) develop and manifest across the age span in individuals with genetic syndromes. In this study we present findings from a two and a half year follow-up of the characteristics associated with ASD in three syndromes: Cornelia de Lange (CdLS), Fragile X (FXS), and Cri du Chat (CdCS). Parents and carers of 251 individuals (CdLS=67, CdCS=42, and FXS=142) completed the Social Communication Questionnaire (SCQ) at Time 1 (T1) and again two and a half years later (T2). The FXS and CdLS groups were more likely to meet the cut-offs for both autism and ASD and show greater severity of ASD related behaviors, at both T1 and T2, compared to the CdCS group. Older individuals (>15yrs) with CdLS were more likely to meet the cut off for ASD than younger individuals (≤15 yrs) with the syndrome and more likely to show greater severity of social impairments. In FXS repetitive behaviors were found to become less prominent with age and in CdCS social impairments were reported to be more severe with age. There were no significant changes between T1 and T2 in the severity of ASD characteristics in the CdCS and CdLS groups. The FXS group showed significantly fewer repetitive behaviors and less severe impairments in social interaction over this time frame. The findings suggest that while there may be similarities in overall severity and presentation of ASD characteristics in CdLS and FXS, these characteristics have divergent patterns of development within these groups.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  Cornelia de Lange syndrome; Cri du Chat syndrome; Fragile X syndrome; autism; autism spectrum disorder; behavioral phenotype; follow-up; longitudinal

Mesh:

Year:  2015        PMID: 25989416     DOI: 10.1002/ajmg.c.31438

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  9 in total

Review 1.  Behavioral and psychiatric manifestations in Cornelia de Lange syndrome.

Authors:  Marco A Grados; Mustafa H Alvi; Siddharth Srivastava
Journal:  Curr Opin Psychiatry       Date:  2017-03       Impact factor: 4.741

2.  Restricted and Repetitive Behaviors in Males and Females with Fragile X Syndrome: Developmental Trajectories in Toddlers Through Young Adults.

Authors:  Lauren J Moskowitz; Elizabeth A Will; Conner J Black; Jane E Roberts
Journal:  J Autism Dev Disord       Date:  2020-11

Review 3.  Updated report on tools to measure outcomes of clinical trials in fragile X syndrome.

Authors:  Dejan B Budimirovic; Elizabeth Berry-Kravis; Craig A Erickson; Scott S Hall; David Hessl; Allan L Reiss; Margaret K King; Leonard Abbeduto; Walter E Kaufmann
Journal:  J Neurodev Disord       Date:  2017-06-12       Impact factor: 4.025

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.  Using Bayesian methodology to explore the profile of mental health and well-being in 646 mothers of children with 13 rare genetic syndromes in relation to mothers of children with autism.

Authors:  Dawn Adams; Richard P Hastings; Clair Alston-Knox; Rina Cianfaglione; Kate Eden; David Felce; Gemma Griffith; Jo Moss; Chris Stinton; Chris Oliver
Journal:  Orphanet J Rare Dis       Date:  2018-10-25       Impact factor: 4.123

7.  Movement Disorders and Syndromic Autism: A Systematic Review.

Authors:  L Bell; A Wittkowski; D J Hare
Journal:  J Autism Dev Disord       Date:  2019-01

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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