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Results 1 - 10 of 14 for Cerebral inclusion bodies
  1. Familial encephalopathy with neuroserpin inclusion bodies 
    Familial encephalopathy with neuroserpin inclusion bodies (FENIB) is a disorder that causes progressive dysfunction of the brain (encephalopathy). It is characterized by a loss of intellectual functioning (dementia) and seizures. At first, affected individuals may have difficulty ...
    https://medlineplus.gov/...lopathy-with-neuroserpin-inclusion-bodies - Genetics
  2. Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 
    Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (IBMPFD) is a condition that can affect the muscles, bones, and brain.The first symptom of IBMPFD is often muscle weakness (myopathy), which typically appears in mid-adulthood. ...
    https://medlineplus.gov/...paget-disease-and-frontotemporal-dementia - Genetics
  3. SERPINI1 gene 
    ... to one another and form clumps called neuroserpin inclusion bodies or Collins bodies. These clumps disrupt the cells' normal functioning and ultimately lead to cell death. The gradual loss of neurons in certain parts of the brain causes progressive dementia in people with FENIB.SERPINI1 ...
    https://medlineplus.gov/genetics/gene/serpini1 - Genetics
  4. VCP gene 
    ... gene have been identified in people who have inclusion body myopathy with ... a brain condition called frontotemporal dementia that worsens over time. ...
    https://medlineplus.gov/genetics/gene/vcp - Genetics
  5. Fragile X-associated tremor/ataxia syndrome 
    ... found in clumps of proteins and mRNA (intranuclear inclusions) in brain and nerve cells in people with FXTAS. It is thought that attaching to FMR1 mRNA and forming clumps keeps the other proteins ... inclusions is unclear. In addition, the repeat expansion makes ...
    https://medlineplus.gov/...agile-x-associated-tremor-ataxia-syndrome - Genetics
  6. Dementia with Lewy bodies 
    ... Rempala G, Sadee W. Gene expression profiling of brain samples from patients with Lewy body dementia. Biochem Biophys Res Commun. 2016 Oct 28; ...
    https://medlineplus.gov/genetics/condition/dementia-with-lewy-bodies - Genetics
  7. Multiple system atrophy 
    ... up in cells in many parts of the brain and spinal cord. Over time, these clumps (which are known as inclusions) damage cells in parts of the nervous system ...
    https://medlineplus.gov/genetics/condition/multiple-system-atrophy - Genetics
  8. HTT gene 
    ... birth. Huntingtin is found in many of the body's tissues, with the highest levels of activity in the brain. Within cells, this protein may be involved in ...
    https://medlineplus.gov/genetics/gene/htt - Genetics
  9. ARX gene 
    ... embryonic development to control the formation of many body structures. Specifically, the ARX protein is believed to be involved in the development of the brain, pancreas, testes, and muscles used for movement (skeletal ...
    https://medlineplus.gov/genetics/gene/arx - Genetics
  10. GRN-related frontotemporal lobar degeneration 
    ... is active in many different tissues in the body, where it helps control the growth, division, and survival of cells. Progranulin's function in the brain is not well understood, although it appears to ...
    https://medlineplus.gov/...related-frontotemporal-lobar-degeneration - Genetics
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