ADan amyloidosis

MONDO:0007297

A cerebral amyloid angiopathy characterized by ataxia, intention tremor, psychosis and dementia that has material basis in an autosomal dominant mutation of ITM2B on chromosome 13q14.2.

Also known as: FDD, HOOE, Heredopathia Ophthalmootoencephalica, cerebellar ataxia, cataract, deafness, and dementia Or psychosis, cerebral amyloid angiopathy, ITM2B-related, type 2, familial Danish dementia, familial dementia, Danish type, ITM2B-related cerebral amyloid angiopathy 2

13 clinical trials for this condition and its sub-types, 0 tagged with ADan amyloidosis itself.

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↑ Cerebral amyloid angiopathy (17) ↑ ITM2B amyloidosis (0)

Including sub-types (13) Tagged with ADan amyloidosis (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.