Corpus callosum metrics predict severity of visuospatial and neuromotor dysfunctions in ARID1B mutations with Coffin-Siris syndrome

被引:10
作者
Demily, Caroline [1 ,2 ]
Duwime, Charlyne [3 ]
Lopez, Clemence [4 ,5 ,6 ]
Hemimou, Cherhazad [4 ,5 ,6 ]
Poisson, Alice [1 ,2 ]
Plasse, Julien [7 ,8 ,9 ,10 ]
Robert, Matthieu P. [11 ,12 ]
Denier, Charlotte [11 ,12 ]
Rossi, Massimiliano [13 ,14 ]
Franck, Nicolas [7 ,8 ,9 ,10 ]
Besmond, Claude [15 ]
Barcia, Giulia [16 ]
Boddaert, Nathalie [17 ,18 ]
Munnich, Arnold [16 ]
Vaivre-Douret, Laurence [4 ,5 ,6 ]
机构
[1] le Vinatier Hosp, Reference Ctr Rare Dis Psychiat Phenotype GenoPsy, Bron, France
[2] Marc Jeannerod Inst, Bron, France
[3] Fondat Elan Retrouve & Inst Imagine, Paris, France
[4] Univ Paris 05, Fac Med, SPC, Paris, France
[5] Univ Paris Sud Paris Saclay, UVSO Villejuif & Paris Descartes, INSERM, UMR 1178,1018 CESP,SPC, Paris, France
[6] Necker Enfants Malad Univ Hosp, AP HP, Paris, France
[7] CRR, Psychosocial Rehabil & Cognit Remediat Ressource, Bron, France
[8] le Vinatier Hosp, SUR CL3R, Bron, France
[9] CNRS, Marc Jeannerod Inst, UMR 5229, Bron, France
[10] Claude Bernard Lyon 1 Univ, Bron, France
[11] Necker Enfants Malad Univ Hosp, AP HP, Ophthalmol Dept, Paris, France
[12] Paris Descartes Univ, Sorbonne, Paris, France
[13] Hosp Civils Lyon, Genet Dept, Bron, France
[14] Claude Bernard Lyon 1 Univ, Lyon Neurosci Res Ctr, GENDEV Team, CNRS,INSERM 01028,UMR 5292, Bron, France
[15] Inst Imagine, Genet Translat, INSERM, UMR1163, Paris, France
[16] Paris Descartes Univ, Necker Hosp, Genet Dept, INSERM,UMR 1163, Paris, France
[17] Univ Paris 05, Hop Necker Enfants Malad, AP HP, INSERM,UMR 1163,Inst Imagine,Pediat Radiol Dept,P, Paris, France
[18] INSERM U1000, Paris, France
关键词
ARID1B; autism spectrum disorder; Coffin-Siris syndrome; corpus callosum; neuromotor; visuospatial; HAPLOINSUFFICIENCY; MORPHOLOGY; COMPLEX;
D O I
10.1097/YPG.0000000000000225
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
ARID1B mutations in Coffin-Siris syndrome are a cause of intellectual disability (0.5-1%), with various degrees of autism and agenesis of the corpus callosum (10%). Little is known regarding the cognitive and motor consequences of ARID1B mutations in humans and no link has been made between corpus callosum anomalies and visuospatial and neuromotor dysfunctions. We have investigated the visuospatial and neuromotor phenotype in eight patients with ARID1B mutations. A paramedian sagittal section of the brain MRI was selected, and corpus callosum was measured in anteroposterior length, genu and trunk width. Spearman's rank order coefficients were used to explore correlations between visuospatial and social cognitive variables and dimensions of the corpus callosum. A significant correlation between genu width size and visual cognition was observed. Retrocerebellar cysts were associated with corpus callosum anomalies. Here, we show that corpus callosum anomalies caused in ARID1B mutations may be predictive of the visuospatial and motor phenotype in Coffin-Siris syndrome. Copyright (C) 2019 Wolters Kluwer Health. Inc. All rights reserved.
引用
收藏
页码:237 / 242
页数:6
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