Familial encephalopathy with neuroserpin inclusion bodies

A neurodegenerative disease that is characterized by intraneuronal inclusions of mutant neuroserpin resulting in progressive encephalopathy, dementia and seizures and has material basis in a mutation in the SERPINI1 gene inherited in an in autosomal dominant pattern.

Also known as: FENIB, encephalopathy, familial, with Collins bodies, encephalopathy, familial, with neuroserpin inclusion bodies

7 clinical trials for this condition and its sub-types, 0 tagged with Familial encephalopathy with neuroserpin inclusion bodies itself.