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目的通过舞蹈-棘红细胞增多症(ChAc)的临床资料分析,提高对ChAc的认识。方法对收治的1例ChAc病例的诊断过程进行分析,结合文献复习对神经棘红细胞增多症(NA)的遗传方式、影像学和实验室检查等特点进行总结。结果NA临床症状复杂多样,其发病特点与广泛的非特异性神经系统病变、棘红细胞增多密切相关。NA治疗以对症支持为主。结论NA是一种罕见的神经退行性疾病,预后差;早发现、早诊断、早治疗可改善预后。
Objective To improve the understanding of ChAc through the clinical data analysis of chorea-acanthocytosis (ChAc). Methods One case of ChAc admitted to our hospital was diagnosed. The literature reviewed the genetic patterns of neuro - acanthosis (NA), imaging and laboratory tests. Results The clinical features of NA were complex and diverse. The features of NA were closely related to the extensive nonspecific neurological diseases and the increase of erythrocytes. NA treatment with symptomatic support based. Conclusion NA is a rare neurodegenerative disease with poor prognosis. Early detection, early diagnosis and early treatment can improve the prognosis.