Steinlin M, Schmitt B, Ferrini B
Division of Neurology, University Children's Hospital, Zurich, Switzerland.
Brain Dev. 1998 Jun;20(4):242-4. doi: 10.1016/s0387-7604(98)00021-7.
Congenital cerebellar ataxia is usually thought to be of cerebellar origin. We report two children with congenital cerebellar ataxia, in whom neuroimaging investigations suggest the possibility of a parietal etiology. The two boys showed hypotonia, delayed motor and cognitive development followed by marked, truncally pronounced ataxia. In one case infantile spasms were treated successfully with adrenocorticotropic hormone, although in follow-up the child suffered from occasional seizures. Magnetic resonance imaging showed in one case parieto-occipital pachygyria and in the other there was marked pachygyria, most pronounced over the parieto-occipital area. In both children cerebellar structures were normal. Cerebello-parietal connections are known to be responsible for acquired parietal limb ataxia. Although not proven, parietal lesions are the most likely etiology of congenital cerebellar ataxia in these two children. Therefore, cerebral, especially parietal pathology must be considered in children with congenital ataxia.
先天性小脑共济失调通常被认为起源于小脑。我们报告了两名患有先天性小脑共济失调的儿童,神经影像学检查提示可能存在顶叶病因。这两名男孩表现为肌张力减退、运动和认知发育迟缓,随后出现明显的、以躯干为主的共济失调。在其中一例中,婴儿痉挛症用促肾上腺皮质激素成功治疗,尽管在随访中该儿童偶尔仍有癫痫发作。磁共振成像显示,一例为顶枕叶巨脑回,另一例有明显的巨脑回,在顶枕叶区域最为明显。两名儿童的小脑结构均正常。已知小脑 - 顶叶连接负责后天性顶叶肢体共济失调。虽然尚未得到证实,但顶叶病变是这两名儿童先天性小脑共济失调最可能的病因。因此,对于患有先天性共济失调的儿童,必须考虑脑部,尤其是顶叶病变。