Literature DB >> 25524843

A prospective longitudinal study on visuo-cognitive development in Dravet syndrome: Is there a "dorsal stream vulnerability"?

D Ricci1, D Chieffo1, D Battaglia1, C Brogna1, I Contaldo1, V De Clemente1, E Losito1, Ch Dravet1, E Mercuri1, F Guzzetta2.   

Abstract

A group of five DS patients whose first development was already reported were longitudinally followed up till the scholar age. Beside the general and epileptic clinical evolution, visual and cognitive functions were investigated in order to define their trajectory and possibly provide information about mechanisms of cognitive decline as well as to improve prognosis and tertiary prevention. Neuropsychological assessment was performed with a test battery investigating the development of visual function that progressively integrates into extrastriate components and higher cognitive skills (global form and motion coherence, stereopsis, crowding cards, ABCDEFV battery, general intelligence and specific cognitive tests). Main results showed a fall in visuo-motor items including global motion coherence and specific cognitive skills, presenting a continuity of the visual function deterioration extended from basic abilities to visuo-motor dorsal pathway skills. Moreover, a case whose previous visual and cognitive functions had been in the normal range began showing a visual deterioration with increasing age, followed by the cognitive decline; that prevents from excluding in early ages a poor development in presence of a normal visual function. A dorsal stream vulnerability seems thus shown in this sample of DS patients, like in other genetic syndromes (Williams, Prader Willi. fragile-X), providing new information about mechanisms underlying cognitive decline and suggesting a possible strategy to improve their neuropsychological outcome. Larger cohorts may confirm whether these findings are part of a specific pattern of DS neuropsychological phenotype.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Dorsal stream processing; Dravet syndrome; Early development; Visual function

Mesh:

Year:  2014        PMID: 25524843     DOI: 10.1016/j.eplepsyres.2014.10.009

Source DB:  PubMed          Journal:  Epilepsy Res        ISSN: 0920-1211            Impact factor:   3.045


  4 in total

1.  Global motion perception is related to motor function in 4.5-year-old children born at risk of abnormal development.

Authors:  Arijit Chakraborty; Nicola S Anstice; Robert J Jacobs; Nabin Paudel; Linda L LaGasse; Barry M Lester; Christopher J D McKinlay; Jane E Harding; Trecia A Wouldes; Benjamin Thompson
Journal:  Vision Res       Date:  2017-04-28       Impact factor: 1.886

2.  Cerebral visual impairment in CDKL5 deficiency disorder: vision as an outcome measure.

Authors:  Heather E Olson; Julia G Costantini; Lindsay C Swanson; Walter E Kaufmann; Timothy A Benke; Anne B Fulton; Ronald Hansen; Annapurna Poduri; Gena Heidary
Journal:  Dev Med Child Neurol       Date:  2021-05-24       Impact factor: 5.449

3.  Autism spectrum disorder and cognitive profile in children with Dravet syndrome: Delineation of a specific phenotype.

Authors:  Lisa Ouss; Dorothee Leunen; Jacques Laschet; Nicole Chemaly; Giulia Barcia; Emma M Losito; Aveline Aouidad; Zoe Barrault; Isabelle Desguerre; Delphine Breuillard; Rima Nabbout
Journal:  Epilepsia Open       Date:  2018-12-20

4.  Visual Function and Ophthalmological Findings in CHARGE Syndrome: Revision of Literature, Definition of a New Clinical Spectrum and Genotype Phenotype Correlation.

Authors:  Roberta Onesimo; Daniela Ricci; Cristiana Agazzi; Simona Leone; Maria Petrianni; Lorenzo Orazi; Filippo Amore; Annabella Salerni; Chiara Leoni; Daniela Chieffo; Marco Tartaglia; Eugenio Mercuri; Giuseppe Zampino
Journal:  Genes (Basel)       Date:  2021-06-25       Impact factor: 4.096

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.