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Adult-onset neuronal intranuclear hyaline inclusion disease.

Authors
  • Munoz-Garcia, D
  • Ludwin, S K
Type
Published Article
Journal
Neurology
Publication Date
Jun 01, 1986
Volume
36
Issue
6
Pages
785–790
Identifiers
PMID: 3010181
Source
Medline
License
Unknown

Abstract

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.

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