Literature DB >> 27164360

Cornelia de Lange syndrome: Correlation of brain MRI findings with behavioral assessment.

Tamanna R Roshan Lal, Mark A Kliewer, Thelma Lopes, Susan L Rebsamen, Julia O'Connor, Marco A Grados, Amy Kimball, Julia Clemens, Antonie D Kline.   

Abstract

Neurobehavioral and developmental issues with a broad range of deficits are prominent features of Cornelia de Lange syndrome (CdLS), a disorder due to disruption of the cohesin protein complex. The etiologic relationship of these clinical findings to anatomic abnormalities on neuro-imaging studies has not, however, been established. Anatomic abnormalities in the brain and central nervous system specific to CdLS have been observed, including changes in the white matter, brainstem, and cerebellum. We hypothesize that location and severity of brain abnormalities correlate with clinical phenotype in CdLS, as seen in other developmental disorders. In this study, we retrospectively evaluated brain MRI studies of 15 individuals with CdLS and compared these findings to behavior at the time of the scan. Behavior was assessed using the Aberrant Behavior Checklist (ABC), a validated behavioral assessment tool with several clinical features. Ten of fifteen (67%) of CdLS patients had abnormal findings on brain MRI, including cerebral atrophy, white matter changes, cerebellar hypoplasia, and enlarged ventricles. Other findings included pituitary tumors or cysts, Chiari I malformation and gliosis. Abnormal behavioral scores in more than one behavioral area were seen in all but one patient. All 5 of the 15 (33%) patients with normal structural MRI studies had abnormal ABC scores. All normal ABC scores were noted in only one patient and this was correlated with moderately abnormal MRI changes. Although our cohort is small, our results suggest that abnormal behaviors can exist in individuals with CdLS in the setting of relatively normal structural brain findings.
© 2016 Wiley Periodicals, Inc. © 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  Aberrant Behavior Checklist; Cornelia de Lange syndrome; MRI; behavior; brain

Mesh:

Year:  2016        PMID: 27164360      PMCID: PMC5446089          DOI: 10.1002/ajmg.c.31503

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


  35 in total

1.  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

2.  Autism traits in children and adolescents with Cornelia de Lange syndrome.

Authors:  Siddharth Srivastava; Colleen Landy-Schmitt; Bennett Clark; Antonie D Kline; Matt Specht; Marco A Grados
Journal:  Am J Med Genet A       Date:  2014-04-09       Impact factor: 2.802

3.  Behavioural phenotype of Cornelia de Lange syndrome: case-control study.

Authors:  Chris Oliver; Kate Arron; Jenny Sloneem; Scott Hall
Journal:  Br J Psychiatry       Date:  2008-12       Impact factor: 9.319

Review 4.  Natural history of aging in Cornelia de Lange syndrome.

Authors:  Antonie D Kline; Marco Grados; Paul Sponseller; Howard P Levy; Natalie Blagowidow; Christianne Schoedel; Joni Rampolla; Douglas K Clemens; Ian Krantz; Amy Kimball; Carmen Pichard; David Tuchman
Journal:  Am J Med Genet C Semin Med Genet       Date:  2007-08-15       Impact factor: 3.908

5.  The behavioural phenotype of Cornelia de Lange Syndrome: a study of 56 individuals.

Authors:  E Basile; L Villa; A Selicorni; M Molteni
Journal:  J Intellect Disabil Res       Date:  2007-09

6.  The contribution of cohesin-SA1 to gene expression and chromatin architecture in two murine tissues.

Authors:  Ana Cuadrado; Silvia Remeseiro; Osvaldo Graña; David G Pisano; Ana Losada
Journal:  Nucleic Acids Res       Date:  2015-03-03       Impact factor: 16.971

7.  Sylvian fissure and parietal anatomy in children with autism spectrum disorder.

Authors:  Tracey A Knaus; Helen Tager-Flusberg; Anne L Foundas
Journal:  Behav Neurol       Date:  2012       Impact factor: 3.342

8.  NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome.

Authors:  Emma T Tonkin; Tzu-Jou Wang; Steven Lisgo; Michael J Bamshad; Tom Strachan
Journal:  Nat Genet       Date:  2004-05-16       Impact factor: 38.330

9.  HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle.

Authors:  Matthew A Deardorff; Masashige Bando; Ryuichiro Nakato; Erwan Watrin; Takehiko Itoh; Masashi Minamino; Katsuya Saitoh; Makiko Komata; Yuki Katou; Dinah Clark; Kathryn E Cole; Elfride De Baere; Christophe Decroos; Nataliya Di Donato; Sarah Ernst; Lauren J Francey; Yolanda Gyftodimou; Kyotaro Hirashima; Melanie Hullings; Yuuichi Ishikawa; Christian Jaulin; Maninder Kaur; Tohru Kiyono; Patrick M Lombardi; Laura Magnaghi-Jaulin; Geert R Mortier; Naohito Nozaki; Michael B Petersen; Hiroyuki Seimiya; Victoria M Siu; Yutaka Suzuki; Kentaro Takagaki; Jonathan J Wilde; Patrick J Willems; Claude Prigent; Gabriele Gillessen-Kaesbach; David W Christianson; Frank J Kaiser; Laird G Jackson; Toru Hirota; Ian D Krantz; Katsuhiko Shirahige
Journal:  Nature       Date:  2012-09-13       Impact factor: 49.962

Review 10.  Congenital hypoplasia of the cerebellum: developmental causes and behavioral consequences.

Authors:  M Albert Basson; Richard J Wingate
Journal:  Front Neuroanat       Date:  2013-09-03       Impact factor: 3.856

View more
  6 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.  Lithium as a possible therapeutic strategy for Cornelia de Lange syndrome.

Authors:  Paolo Grazioli; Chiara Parodi; Milena Mariani; Daniele Bottai; Elisabetta Di Fede; Aida Zulueta; Laura Avagliano; Anna Cereda; Romano Tenconi; Jolanta Wierzba; Raffaella Adami; Maria Iascone; Paola Francesca Ajmone; Thomas Vaccari; Cristina Gervasini; Angelo Selicorni; Valentina Massa
Journal:  Cell Death Discov       Date:  2021-02-17

3.  Rings and Bricks: Expression of Cohesin Components is Dynamic during Development and Adult Life.

Authors:  Laura Rachele Bettini; Federica Graziola; Grazia Fazio; Paolo Grazioli; Valeria Scagliotti; Mariavittoria Pasquini; Giovanni Cazzaniga; Andrea Biondi; Lidia Larizza; Angelo Selicorni; Carles Gaston-Massuet; Valentina Massa
Journal:  Int J Mol Sci       Date:  2018-02-01       Impact factor: 5.923

Review 4.  Integrating molecular and structural findings: Wnt as a possible actor in shaping cognitive impairment in Cornelia de Lange syndrome.

Authors:  Laura Avagliano; Paolo Grazioli; Milena Mariani; Gaetano P Bulfamante; Angelo Selicorni; Valentina Massa
Journal:  Orphanet J Rare Dis       Date:  2017-11-21       Impact factor: 4.123

Review 5.  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

Review 6.  Analysis of clinical and genetic characteristics in 10 Chinese individuals with Cornelia de Lange syndrome and literature review.

Authors:  Chen Liu; Xiaoying Li; Jing Cui; Rui Dong; Yvqiang Lv; Dong Wang; Haiyan Zhang; Xiaomei Li; Zilong Li; Jian Ma; Yi Liu; Zhongtao Gai
Journal:  Mol Genet Genomic Med       Date:  2020-08-27       Impact factor: 2.183

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.