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familial encephalopathy with neuroserpin inclusion bodies
Pathology:
- unique neuronal inclusion bodies of neuroserpin polymers
Genetics:
- autosomal dominant
- associated with defects in SERPINI1
Clinical manifestations:
- dementia
General
encephalopathy
genetic disease of the central nervous system
Database Correlations
OMIM 604218
References
OMIM :accession 604218