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Results 1 - 6 of 6 for Genetic neurodegenerative disease with dementia
  1. Familial encephalopathy with neuroserpin inclusion bodies 
    ... person has a parent with the condition. Familial dementia with ... associated with a recently reported familial neurodegenerative disease: familial encephalopathy with neuroserpin inclusion bodies. Arch Neurol. ...
    https://medlineplus.gov/...lopathy-with-neuroserpin-inclusion-bodies - Genetics
  2. Prion disease 
    ... diseases Prion-associated disorders Prion-induced disorders Transmissible dementias Transmissible spongiform encephalopathies TSEs Genetic Testing Registry: Fatal familial insomnia Genetic Testing Registry: ...
    https://medlineplus.gov/genetics/condition/prion-disease - Genetics
  3. Aceruloplasminemia 
    ... M, Fuchs R, Harris ZL. Aceruloplasminemia: an inherited neurodegenerative disease with impairment of iron homeostasis. Ann N Y Acad Sci. 2004 Mar;1012:299-305. doi: 10.1196/annals.1306.024. Citation on PubMed
    https://medlineplus.gov/genetics/condition/aceruloplasminemia - Genetics
  4. Neuroferritinopathy 
    ... accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide gene. J Neuropathol Exp Neurol. 2004 Apr;63(4):363-80. doi: 10.1093/jnen/63.4.363. Citation on PubMed
    https://medlineplus.gov/genetics/condition/neuroferritinopathy - Genetics
  5. Progressive supranuclear palsy 
    ... For example, the disease has been linked to genetic changes on chromosome 1 and chromosome 11. However, ... a loss of intellectual functions (dementia).When progressive supranuclear palsy runs in families, it ...
    https://medlineplus.gov/.../condition/progressive-supranuclear-palsy - Genetics
  6. Infantile neuroaxonal dystrophy 
    ... this disorder experience progressive deterioration of cognitive functions (dementia), and they eventually lose awareness of their surroundings. ... to have mutations in the PLA2G6 gene. The genetic cause of the condition in these cases is ...
    https://medlineplus.gov/.../infantile-neuroaxonal-dystrophy - Genetics