自Estes等1967年首次报告后,伴棘细胞症的肌萎缩性舞蹈病已有五个家系的报告。其主要症状为精神改变、舞蹈样不自主运动、肢体肌肉萎缩和棘细胞症。作者报导一个家系,四例,其中一例有神经病学、儿茶酚胺等生化分析以及红细胞膜异常性质的实验研究。 Since Estes et al. First reported in 1967, there have been five pedigrees reported with amyotrophic achondropathies. The main symptoms are mental changes, dance-like involuntary movements, limb muscle atrophy and spinocytosis. The authors report a pedigree, four cases, one case of neurology, catecholamine and other biochemical analysis and the nature of the abnormal erythrocyte membrane experimental study.