1 / 1
|
DeCS
|
|
|
Descriptor Inglés:
|
|
TDP-43 Proteinopathies
|
Descriptor Español:
|
|
Proteinopatías TDP-43
|
Descriptor Portugués:
|
|
Proteinopatias TDP-43
|
Sinónimos Inglés:
|
|
Proteinopathies, TDP-43
Proteinopathy, TDP-43
TDP 43 Proteinopathies
TDP-43 Proteinopathy
|
Categoría:
|
|
C10.574.950
C18.452.845.800
|
Definición Inglés:
|
|
Diseases characterized by the presence of abnormally phosphorylated, ubiquitinated, and cleaved DNA-binding protein TDP-43 in affected brain and spinal cord. Inclusions of the pathologic protein in neurons and glia, without the presence of AMYLOID, is the major feature of these conditions, thus making these proteinopathies distinct from most other neurogenerative disorders in which protein misfolding leads to brain amyloidosis. Both frontotemporal lobar degeneration and AMYOTROPHIC LATERAL SCLEROSIS exhibit this common method of pathogenesis and thus they may represent two extremes of a continuous clinicopathological spectrum of one disease. |
Nota Histórica Inglés:
|
|
2010
|
Calificadores Permitidos Inglés:
|
|
|
Número del Registro:
|
|
53517
|
Identificador Único:
|
|
D057177
|
Ocurrencia en la BVS:
|
|
|
Similar:
|
|
DeCS CID-10 SciELO LILACS LIS
|