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一名自闭症儿童患双侧牵牛花综合征并伴有中线脑病变。

Bilateral morning glory syndrome with midline brain lesion in an autistic child.

作者信息

Nawratzki I, Schwartzenberg T, Zaubermann H, Yanko L

机构信息

Michaelson Institute for the Prevention of Blindness, Jerusalem, Israel.

出版信息

Metab Pediatr Syst Ophthalmol (1985). 1985;8(2-3):35-6.

PMID:3870943
Abstract

A ten-year-old autistic boy with high myopia and very poor vision presented a bilateral anomaly of the disc, diagnosed as morning glory syndrome. Further investigation showed an absence of the corpus callosum and probably herniation of an encephalocele into the third ventricle. The association of bilateral morning glory syndrome and very low visual acuity in both eyes with a midline brain lesion and autism has not been previously described.

摘要

一名患有高度近视且视力极差的10岁自闭症男孩出现双侧视盘异常,被诊断为牵牛花综合征。进一步检查显示胼胝体缺失,可能有脑膨出疝入第三脑室。双侧牵牛花综合征、双眼极低视力与中线脑病变及自闭症的关联此前尚未有过描述。

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