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Language Impairment with a Partial Duplication of DOCK8
被引:2
作者:
Benitez-Burraco, Antonio
[1
]
Fernandez-Urquiza, Maite
[2
]
Jimenez-Romero, Ma Salud
[3
]
机构:
[1] Univ Seville, Dept Spanish Linguist & Theory Literature Linguis, Seville, Spain
[2] Univ Oviedo, Dept Spanish Philol, Oviedo, Spain
[3] Univ Cordoba, Dept Educ, Cordoba, Spain
关键词:
9p24;
3;
duplication;
DOCK8;
Cognitive delay;
Language deficits;
Working memory;
SLIT;
ROBO;
FOXP2;
REGULATING NEURAL SYSTEMS;
SIGNAL-TRANSDUCTION;
MENTAL-RETARDATION;
CDC42;
GENE;
FOXP2;
EXPRESSION;
AUTISM;
MIGRATION;
CHILDREN;
D O I:
10.1159/000511972
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Duplications of the distal region of the short arm of chromosome 9 are rare, but are associated with learning disabilities and behavioral disturbances. We report in detail the cognitive and language features of a child with a duplication in the 9p24.3 region, arr[hg19] 9p24.3(266,045-459,076)x3. The proband exhibits marked expressive and receptive problems, which affect both structural and functional aspects of language. These problems might result from a severe underlying deficit in working memory. Regarding the molecular causes of the observed symptoms, they might result from the altered expression of selected genes involved in procedural learning, particularly some of components of the SLIT/ROBO/FOXP2 network, strongly related to the development and evolution of language. Dysregulation of specific components of this network can result in turn from an altered interaction between DOCK8, affected by the microduplication, and CDC42, acting as the hub component of the network encompassing language-related genes.
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页码:243 / 263
页数:21
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