Friede R L, Boltshauser E
Dev Med Child Neurol. 1978 Dec;20(6):758-63. doi: 10.1111/j.1469-8749.1978.tb15307.x.
Necropsy findings are reported for a case of Joubert syndrome (familiar aplasia of cerebellar vermis with episodic hyperpnea, abnormal eye-movements, ataxia and retardation). The findings consisted of an almost total aplasia of the cerebellar vermis; dysplasias and numerous heterotopias of cerebellar nuclei; an almost total absence of pyramidal decussation; and anomalies in the structure of the inferior olivary nuclei, the descending trigeminal tract, solitary fascicle and of the dorsal column nuclei. The lesion resembled the Dandy-Walker malformation or simple aplasia of the cerebellar vermis in some of its aspects, but there were numerous others to set it apart--at least tentatively--as a distinct nosologic entity.
本文报告了一例Joubert综合征(家族性小脑蚓部发育不全伴发作性呼吸急促、异常眼球运动、共济失调和智力发育迟缓)的尸检结果。结果包括小脑蚓部几乎完全发育不全;小脑核发育异常和大量异位;锥体交叉几乎完全缺失;下橄榄核、三叉神经下行束、孤束和薄束核结构异常。该病变在某些方面类似于Dandy-Walker畸形或单纯小脑蚓部发育不全,但也有许多其他特征使其至少暂时作为一种独特的疾病实体与之区分开来。