Literature DB >> 18387531

Cerebellar cognitive affective syndrome without global mental retardation in two relatives with Gillespie syndrome.

Peter Mariën1, Raf Brouns, Sebastiaan Engelborghs, Peggy Wackenier, Jo Verhoeven, Berten Ceulemans, Peter P De Deyn.   

Abstract

Although previous studies of Gillespie syndrome have systematically reported a generalized delay of cognitive development (mental retardation or oligophrenia), psychometric data to substantiate this view are strikingly absent. In the present study two first degree relatives (mother and daughter) with Gillespie syndrome were neuropsychologically investigated. Aside from a marked asymmetry in the Wechsler-IQ profile, consisting of significantly better results on the verbal [Verbal IQ (VIQ)] than on the nonverbal part [Performance IQ (PIQ)] of the test, cognitive and behavioral assessments revealed a pattern of abnormalities that closely resembles the "cerebellar cognitive and affective syndrome" (CeCAS) (Schmahmann and Sherman, 1998). Aside from prefrontal dysexecutive dysfunctions such as disturbed cognitive planning and set-shifting, parietal lobe involvement was reflected by impaired visuo-spatial memory and visuo-spatial disorganization in constructional tasks. Within the linguistic domain involvement of the prefrontal and temporal language regions was indicated by impaired letter fluency, incidences of agrammatism, apraxia of speech and disrupted language dynamics. With regard to mood and behavior, a number of personality and affective characteristics were found that are typically associated with prefrontal lobe damage and dysfunction of limbic related regions in the cingulate and parahippocampal gyri. Disinhibited symptoms characterized behavior and affect of the mother while the daughter displayed a variety of inhibited symptoms. As a result, behavioral and cognitive findings in these patients do not support the prevailing view of a global mental retardation as a cardinal feature of Gillespie syndrome but primarily reflect cerebellar induced neurobehavioral dysfunctions following disruption of the cerebrocerebellar anatomical circuitry.

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Year:  2007        PMID: 18387531     DOI: 10.1016/j.cortex.2005.12.001

Source DB:  PubMed          Journal:  Cortex        ISSN: 0010-9452            Impact factor:   4.027


  9 in total

1.  GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development.

Authors:  Mats Larsson; David L Duffy; Gu Zhu; Jimmy Z Liu; Stuart Macgregor; Allan F McRae; Margaret J Wright; Richard A Sturm; David A Mackey; Grant W Montgomery; Nicholas G Martin; Sarah E Medland
Journal:  Am J Hum Genet       Date:  2011-08-12       Impact factor: 11.025

2.  Recessive and Dominant De Novo ITPR1 Mutations Cause Gillespie Syndrome.

Authors:  Sylvie Gerber; Kamil J Alzayady; Lydie Burglen; Dominique Brémond-Gignac; Valentina Marchesin; Olivier Roche; Marlène Rio; Benoit Funalot; Raphaël Calmon; Alexandra Durr; Vera Lucia Gil-da-Silva-Lopes; Maria Fernanda Ribeiro Bittar; Christophe Orssaud; Bénédicte Héron; Edward Ayoub; Patrick Berquin; Nadia Bahi-Buisson; Christine Bole; Cécile Masson; Arnold Munnich; Matias Simons; Marion Delous; Helene Dollfus; Nathalie Boddaert; Stanislas Lyonnet; Josseline Kaplan; Patrick Calvas; David I Yule; Jean-Michel Rozet; Lucas Fares Taie
Journal:  Am J Hum Genet       Date:  2016-04-21       Impact factor: 11.025

3.  Developmental coordination disorder: disruption of the cerebello-cerebral network evidenced by SPECT.

Authors:  Peter Mariën; Peggy Wackenier; Didier De Surgeloose; Peter P De Deyn; Jo Verhoeven
Journal:  Cerebellum       Date:  2010-09       Impact factor: 3.847

4.  Altered intra- and interregional synchronization in the absence of the corpus callosum: a resting-state fMRI study.

Authors:  Long Zuo; Shuangkun Wang; Junliang Yuan; Hua Gu; Yang Zhou; Tao Jiang
Journal:  Neurol Sci       Date:  2017-04-24       Impact factor: 3.307

5.  A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect.

Authors:  Meriel McEntagart; Kathleen A Williamson; Jacqueline K Rainger; Ann Wheeler; Anne Seawright; Elfride De Baere; Hannah Verdin; L Therese Bergendahl; Alan Quigley; Joe Rainger; Abhijit Dixit; Ajoy Sarkar; Eduardo López Laso; Rocio Sanchez-Carpintero; Jesus Barrio; Pierre Bitoun; Trine Prescott; Ruth Riise; Shane McKee; Jackie Cook; Lisa McKie; Berten Ceulemans; Françoise Meire; I Karen Temple; Fabienne Prieur; Jonathan Williams; Penny Clouston; Andrea H Németh; Siddharth Banka; Hemant Bengani; Mark Handley; Elisabeth Freyer; Allyson Ross; Veronica van Heyningen; Joseph A Marsh; Frances Elmslie; David R FitzPatrick
Journal:  Am J Hum Genet       Date:  2016-04-21       Impact factor: 11.025

6.  Identification of novel and hotspot mutations in the channel domain of ITPR1 in two patients with Gillespie syndrome.

Authors:  Maria Lisa Dentici; Sabina Barresi; Marta Nardella; Emanuele Bellacchio; Paolo Alfieri; Alessandro Bruselles; Francesca Pantaleoni; Alberto Danieli; Giancarlo Iarossi; Marco Cappa; Enrico Bertini; Marco Tartaglia; Ginevra Zanni
Journal:  Gene       Date:  2017-07-08       Impact factor: 3.688

7.  Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie Syndrome.

Authors:  Morad Ansari; Jacqueline Rainger; Isabel M Hanson; Kathleen A Williamson; Freddie Sharkey; Louise Harewood; Angela Sandilands; Jill Clayton-Smith; Helene Dollfus; Pierre Bitoun; Francoise Meire; Judy Fantes; Brunella Franco; Birgit Lorenz; David S Taylor; Fiona Stewart; Colin E Willoughby; Meriel McEntagart; Peng Tee Khaw; Carol Clericuzio; Lionel Van Maldergem; Denise Williams; Ruth Newbury-Ecob; Elias I Traboulsi; Eduardo D Silva; Mukhlis M Madlom; David R Goudie; Brian W Fleck; Dagmar Wieczorek; Juergen Kohlhase; Alice D McTrusty; Carol Gardiner; Christopher Yale; Anthony T Moore; Isabelle Russell-Eggitt; Lily Islam; Melissa Lees; Philip L Beales; Stephen J Tuft; Juan B Solano; Miranda Splitt; Jens Michael Hertz; Trine E Prescott; Deborah J Shears; Ken K Nischal; Martine Doco-Fenzy; Fabienne Prieur; I Karen Temple; Katherine L Lachlan; Giuseppe Damante; Danny A Morrison; Veronica van Heyningen; David R FitzPatrick
Journal:  PLoS One       Date:  2016-04-28       Impact factor: 3.240

8.  Gillespie syndrome in a South Asian child: a case report with confirmation of a heterozygous mutation of the ITPR1 gene and review of the clinical and molecular features.

Authors:  Daham De Silva; Kathleen A Williamson; Kavinda Chandimal Dayasiri; Nayani Suraweera; Vinushiya Quinters; Hiranya Abeysekara; Jithangi Wanigasinghe; Deepthi De Silva; Harendra De Silva
Journal:  BMC Pediatr       Date:  2018-09-24       Impact factor: 2.125

Review 9.  The genetic architecture of aniridia and Gillespie syndrome.

Authors:  Hildegard Nikki Hall; Kathleen A Williamson; David R FitzPatrick
Journal:  Hum Genet       Date:  2018-09-22       Impact factor: 4.132

  9 in total

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