Schmidley J W, Levinsohn M W, Manetto V
Neurology. 1987 Aug;37(8):1344-9. doi: 10.1212/wnl.37.8.1344.
We describe an X-linked disorder of the CNS, characterized by onset, in infancy, of hypotonia, ataxia, sensorineural deafness, developmental delay, esotropias, and optic atrophy, and by a progressive course leading to death in childhood. Pathologically, neuron loss and gliosis of the dentate nucleus and inferior olive are conspicuous; involvement of the cerebellar cortex is less prominent. In the proband, the red nucleus, dorsal motor nucleus of the vagus, and central auditory pathways were severely affected. The mother of the proband, now 33, has self-limited episodes of ataxia, and cerebellar atrophy for which no other cause is apparent. The unique heredity, pathology, and clinical picture distinguish this entity from previously described inherited or metabolic ataxias.
我们描述了一种中枢神经系统的X连锁疾病,其特征为婴儿期起病,表现为肌张力减退、共济失调、感音神经性耳聋、发育迟缓、内斜视和视神经萎缩,并呈进行性病程,导致儿童期死亡。病理上,齿状核和下橄榄核的神经元丢失和胶质细胞增生明显;小脑皮质受累较轻。在先证者中,红核、迷走神经背运动核和中枢听觉通路严重受累。先证者的母亲,现年33岁,有自限性共济失调发作和小脑萎缩,无其他明显病因。这种独特的遗传、病理和临床表现将该疾病与先前描述的遗传性或代谢性共济失调区分开来。