Aleksic S, Budzilovich G, Reuben R, Laguna J, Finegold M, McCarthy J, Converse J M, Feigin I
Dev Med Child Neurol. 1975 Aug;17(4):498-504. doi: 10.1111/j.1469-8749.1975.tb03501.x.
The post-mortem examination of the brain of a 2 1/2-year-old girl with clinical featutes of oculo-auriculo-vertebral dysplasia and hemifacial microsomia (Goldenhar-Gorlin syndrom) revealed a unilateral absence of the olfactory foramina of the lamina cribrosa of the ethmoid bone and ipsilateral absence of olfactory bulb and tract. Other cerebral abnormalities were also present. In this report, unilateral arhinencephaly in this disorder has been documented for the first time and an attempt has been made to correlate various nosological, clinical and pathological aspects of the case with previously reported instances of arhinencephaly. It is concluded that unilateral arhinencephaly occurs in a variety of cranial and facial abnormalities and is not specific for any particular syndrome.
对一名患有眼-耳-脊椎发育异常和半侧颜面短小(戈尔登哈-戈林综合征)临床特征的2岁半女孩的大脑进行尸检发现,筛骨筛板的单侧嗅孔缺失,同侧嗅球和嗅束缺失。还存在其他脑部异常。在本报告中,首次记录了该疾病中的单侧无嗅脑畸形,并尝试将该病例的各种疾病分类、临床和病理方面与先前报道的无嗅脑畸形病例相关联。得出的结论是,单侧无嗅脑畸形发生于多种颅面异常中,并非任何特定综合征所特有。