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

More general terms

• encephalopathy
• genetic disease of the central nervous system

Database

• OMIM: https://mirror.omim.org/entry/604218