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Results 1 - 8 of 8 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. 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
  4. 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
  5. 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
  6. 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
  7. Mucolipidosis II alpha/beta 
    ... and symptoms of the condition. I-cell disease Inclusion cell disease MLII Mucolipidosis II Mucolipidosis type II ... cell disease; MRI, MR spectroscopy and neuropathological correlation. Brain Dev. 2012 Oct;34(9):780-3. doi: ...
    https://medlineplus.gov/.../condition/mucolipidosis-ii-alpha-beta - Genetics
  8. Familial hemophagocytic lymphohistiocytosis 
    ... HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5, WITH OR WITHOUT MICROVILLUS INCLUSION DISEASE; FHL5 PubMed Cetica V, Pende D, Griffiths ...
    https://medlineplus.gov/...milial-hemophagocytic-lymphohistiocytosis - Genetics