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Up to: Cerebral amyloid angiopathy · ITM2B amyloidosis
ABri amyloidosis
A cerebral amyloid angiopathy characterized by onset in the 4th to 6th decade of life, progressive mental deterioration, spasticity, muscular rigidity but no tremors, spontaneous movements or sensory changes that has material basis in an autosomal dominant mutation of ITM2B on chromosome 13q14.2.
This condition has no sub-types.