Literature DB >> 21452752

Cognitive and behavioral functioning in Coffin-Siris syndrome and epilepsy: a case presentation.

H Allison Bender1, Charles M Zaroff, Stella Karantzoulis, Luba Nakhutina, William S MacAllister, Daniel Luciano.   

Abstract

The authors characterized the cognitive, adaptive, and behavioral sequelae of Coffin-Siris (CS) syndrome and epilepsy in a 7.5-year-old child. Little is known about the early neurobehavioral presentation of CS. Clinical features consistent with this genetic anomaly include underdeveloped tips and nails of the fifth fingers, extended infranasal depression, and craniofacial abnormalities. MRI findings often reveal callosal agenesis. The authors conducted a neuropsychological evaluation and obtained parental ratings of behavioral and adaptive functioning. Attentional abilities were limited. As assessed by the Mullen Scales of Early Learning, receptive language abilities (age equivalent [AE]: 3-3) were relatively stronger than expressive skills (AE: 1-4). Adaptive functioning was low across all domains (Vineland Adaptive Behavior Composite AE: 1-9). On the Behavior Assessment for Children (BASC-2), social skills dysfunction, stereotyped and self-stimulatory behaviors, restricted interests, ritualistic play, and inappropriate object usage were noted. No significant mood disturbances were endorsed. Study findings indicate a diffuse pattern of neurobehavioral deficits in a child with CS and epilepsy. Further clinical assessment and research should include multidimensional assessment techniques, including evaluation of adaptive behavior, in an effort to capture the full range developmental sequelae in children with CS.

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Year:  2011        PMID: 21452752     DOI: 10.1080/00221325.2010.506604

Source DB:  PubMed          Journal:  J Genet Psychol        ISSN: 0022-1325            Impact factor:   1.509


  2 in total

1.  Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons.

Authors:  Scott Bell; Justine Rousseau; Huashan Peng; Zahia Aouabed; Pierre Priam; Jean-Francois Theroux; Malvin Jefri; Arnaud Tanti; Hanrong Wu; Ilaria Kolobova; Heika Silviera; Karla Manzano-Vargas; Sophie Ehresmann; Fadi F Hamdan; Nuwan Hettige; Xin Zhang; Lilit Antonyan; Christina Nassif; Lina Ghaloul-Gonzalez; Jessica Sebastian; Jerry Vockley; Amber G Begtrup; Ingrid M Wentzensen; Amy Crunk; Robert D Nicholls; Kristin C Herman; Joshua L Deignan; Walla Al-Hertani; Stephanie Efthymiou; Vincenzo Salpietro; Noriko Miyake; Yoshio Makita; Naomichi Matsumoto; Rune Østern; Gunnar Houge; Maria Hafström; Emily Fassi; Henry Houlden; Jolien S Klein Wassink-Ruiter; Dominic Nelson; Amy Goldstein; Tabib Dabir; Julien van Gils; Thomas Bourgeron; Richard Delorme; Gregory M Cooper; Jose E Martinez; Candice R Finnila; Lionel Carmant; Anne Lortie; Renske Oegema; Koen van Gassen; Sarju G Mehta; Dagmar Huhle; Rami Abou Jamra; Sonja Martin; Han G Brunner; Dick Lindhout; Margaret Au; John M Graham; Christine Coubes; Gustavo Turecki; Simon Gravel; Naguib Mechawar; Elsa Rossignol; Jacques L Michaud; Julie Lessard; Carl Ernst; Philippe M Campeau
Journal:  Am J Hum Genet       Date:  2019-04-25       Impact factor: 11.025

2.  Coffin-Siris syndrome and epilepsy.

Authors:  Maria Rosaria Curcio; Silvia Ferranti; Federica Lotti; Salvatore Grosso
Journal:  Neurol Sci       Date:  2020-10-02       Impact factor: 3.307

  2 in total

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