Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR, USA.
J Mov Disord. 2015 Jan;8(1):1-13. doi: 10.14802/jmd.14034. Epub 2015 Jan 13.
Neurodegeneration with brain iron accumulation (NBIA) encompasses a group of inherited disorders that share the clinical features of an extrapyramidal movement disorder accompanied by varying degrees of intellectual disability and abnormal iron deposition in the basal ganglia. The genetic basis of ten forms of NBIA is now known. The clinical features of NBIA range from rapid global neurodevelopmental regression in infancy to mild parkinsonism with minimal cognitive impairment in adulthood, with wide variation seen between and within the specific NBIA sub-type. This review describes the clinical presentations, imaging findings, pathologic features, and treatment considerations for this heterogeneous group of disorders.
神经退行性伴脑铁沉积(NBIA)包括一组遗传性疾病,它们具有锥体外系运动障碍的临床特征,伴有不同程度的智力残疾和基底节铁沉积异常。目前已经确定了十种 NBIA 形式的遗传基础。NBIA 的临床特征范围从婴儿期快速的全面神经发育性退化到成年期轻度帕金森病伴最小认知障碍,在特定的 NBIA 亚型之间和内部都存在广泛的差异。这篇综述描述了这组异质性疾病的临床表现、影像学发现、病理学特征和治疗注意事项。