ADULT-ONSET NEURONAL INTRANUCLEAR HYALINE INCLUSION DISEASE
ADULT-ONSET NEURONAL INTRANUCLEAR HYALINE INCLUSION DISEASE
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DOI：
10.1212/wnl.36.6.785
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发表时间：
1986-06-01
期刊：
影响因子：
9.9
通讯作者：
LUDWIN, SK
中科院分区：
文献类型：
--
作者：
MUNOZGARCIA, D;LUDWIN, SK
我们研究了两例神经元核内透明包涵体病的临床和病理特征。这些病例的独特之处在于发病较晚，表现为痴呆，可能是常染色体显性遗传模式（一名患者），神经胶质细胞内含物占主导地位，以及一些内含物内有矿物质沉积。与其他报告案例的差异表明，这可能不是一个同质实体。
We studied the clinical and pathologic features of two cases of neuronal intranuclear hyaline inclusion disease. The cases were unique in late onset, presentation with dementia, possible autosomal dominant pattern of inheritance (in one patient), predominance of inclusions in glial cells, and mineral deposits within some inclusions. Differences from other reported cases indicate that this is probably not a homogeneous entity.