Familial Alzheimer-like prion disease (Q91713): Difference between revisions
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CID11:ID_1297025427 | |||||||||||||||
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13 August 2026
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Latest revision as of 18:44, 15 August 2026
Familial Alzheimer-like prion disease is an exceedingly rare form of prion disease characterized by the neuropathological features of Alzheimer disease including memory impairment and depression, related to abnormal prion protein (PrP) caused by a pathogenic variant in the PRNP gene. Patients present with a prolonged, atypical course (absence of myoclonus or ataxia) unlike other forms of prion disease with severe neurofibrillary tangle pathology and high levels of cerebral amyloidosis.
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| English | Familial Alzheimer-like prion disease |
Familial Alzheimer-like prion disease is an exceedingly rare form of prion disease characterized by the neuropathological features of Alzheimer disease including memory impairment and depression, related to abnormal prion protein (PrP) caused by a pathogenic variant in the PRNP gene. Patients present with a prolonged, atypical course (absence of myoclonus or ataxia) unlike other forms of prion disease with severe neurofibrillary tangle pathology and high levels of cerebral amyloidosis. |
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CID11:ID_1297025427
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dki-india-ID_1297025427
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Concluído
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13 August 2026
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