Frontal Aslant Tract Abnormality on Diffusion Tensor Imaging in an Aphasic Patient With 49, XXXXY Syndrome

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• 作者：Monica B. Dhakar ; MD ; MS^a ; ^{monicadhakar@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Mohammed Ilyas ; MD^b ; Jeong-Won Jeong ; PhD^b ; Michael E. Behen ; PhD^b ; Harry T. Chugani ; MD^b ; ^{Harry.Chugani@nemours.org" class="auth_mail" title="E-mail the corresponding author}
• 关键词：49 ; XXXXY ; chromosome aneuploidy ; arcuate fasciculus ; language
• 刊名：Pediatric Neurology
• 出版年：2016
• 出版时间：February 2016
• 年：2016
• 卷：55
• 期：Complete
• 页码：64-67
• 全文大小：705 K

文摘

The karyotype 49, XXXXY is one of the most severe forms of chromosome aneuploidy and is characterized clinically by developmental delay and profound language impairment, particularly involving expressive language functions. We describe the neurocognitive profile and structural anatomy of language pathway in a 2-year-old boy with 49, XXXXY syndrome with expressive aphasia.

Methods

Retrospective chart review of the patient was performed. We characterized the language deficits using neuropsychologic testing. We further studied the language pathways using diffusion tensor imaging analytical technique.

Results

The neurocognitive profile of the patient showed relative weakness of expressive language skills compared with other domains. Diffusion tensor imaging analysis demonstrated a poorly developed frontal aslant tract, a weak indirect segment of arcuate fasciculus, and normally developed direct segment of arcuate fasciculus. The frontal aslant tract is a novel pathway that connects the Broca's area with the anterior cingulate and presupplementary motor area and plays a role in the “motor stream” of language.

Conclusion

A poorly developed frontal aslant tract may underlie the expressive language deficits and provide some insight into the role of X chromosome in modulating the development of language tracts.