Bodensteiner J B, Goldblum R M, Goldman A S
Arch Neurol. 1980 Jul;37(7):464-5. doi: 10.1001/archneur.1980.00500560094020.
A 10-year-old boy with ataxia-telangiectasia had severe progressive dystonic posturing that masked the ataxia until treatment relieved the dystonia. A younger sister had mor classical neurologic manifestations of the disease. However, both children had telangiectasia, immunologic abnormalities, and other features of ataxia-telangiectasia. The pathologic changes that have been found in the basal ganglia at autopsy and the occurrence of choreoathetosis, oculomotor disturbances, and now dystonia indicate that the function of the basal ganglia in patients with ataxia-telangiectasia is abnormal. Children who have basal ganglial abnormalities should be studied for ataxia-telangiectasia.
一名患有共济失调-毛细血管扩张症的10岁男孩出现严重的进行性张力障碍姿势,这种姿势掩盖了共济失调,直到治疗缓解了张力障碍。他的妹妹有该疾病更典型的神经学表现。然而,两个孩子都有毛细血管扩张、免疫异常以及共济失调-毛细血管扩张症的其他特征。尸检在基底神经节发现的病理变化以及舞蹈手足徐动症、眼球运动障碍和现在的张力障碍的出现表明,共济失调-毛细血管扩张症患者的基底神经节功能异常。对于有基底神经节异常的儿童,应进行共济失调-毛细血管扩张症的研究。