Language and Literacy Development in Individuals With Velo-cardio-facial Syndrome

被引：6
|
作者：
Antshel, Kevin M. [1 ]
Marrinan, Eileen [2 ]
Kates, Wendy R. [1 ]
Fremont, Wanda [1 ]
Shprintzen, Robert J. [2 ]
机构：
[1] SUNY Upstate Med Univ, Dept Psychiat & Behav Sci, Syracuse, NY 13210 USA
[2] SUNY Upstate Med Univ, Dept Otolaryngol & Commun Sci, Syracuse, NY 13210 USA
来源：
TOPICS IN LANGUAGE DISORDERS | 2009年 / 29卷 / 02期
关键词：
genetic syndrome; language; literacy; 22q11.2 deletion syndrome; VCFS; 22Q11.2 DELETION SYNDROME; SUBMUCOUS CLEFT-PALATE; VELOCARDIOFACIAL SYNDROME VCFS; VASCULAR DISRUPTION SEQUENCE; FUNCTIONAL COMT POLYMORPHISM; SHORT-TERM-MEMORY; OTITIS-MEDIA; WILLIAMS-SYNDROME; NEUROCOGNITIVE PHENOTYPE; PREPULSE INHIBITION;
D O I：
10.1097/TLD.0b013e3181a72084
中图分类号：
H0 [语言学];
学科分类号：
030303 ; 0501 ; 050102 ;
摘要：
Velo-cardio-facial syndrome (VCFS) is a genetic disorder caused by a microdeletion of chromosome 22q11.2. Although there is some variability, VCFS is associated with a characteristic physical, behavioral, and cognitive phenotype. This review article focuses on aspects of language and literacy development in VCFS, describing what is known and offering avenues for future research. The most consistently reported language and literacy findings in the VCFS population include reading, spelling, phonological processing, and auditory verbal rote memory abilities as areas of relative strength. Receptive language abilities are noted to be relatively stronger than expressive language abilities in individuals with VCFS. Speech disorders are very common in VCFS, and the most common compensatory articulation substitution in VCFS is the glottal stop.
引用
收藏
页码：170 / 186
页数：17
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