Search on: TDP-43 PROTEINOPATHIES 
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Descriptor English:   TDP-43 Proteinopathies 
Descriptor Spanish:   Proteinopatías TDP-43 
Descriptor Portuguese:   Proteinopatias TDP-43 
Synonyms English:   Proteinopathies, TDP-43
Proteinopathy, TDP-43
TDP 43 Proteinopathies
TDP-43 Proteinopathy  
Tree Number:   C10.574.950
C18.452.845.800
Definition English:   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. 
History Note English:   2010 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications CN congenital
DI diagnosis DG diagnostic imaging
DH diet therapy DT drug therapy
EC economics EM embryology
EN enzymology EP epidemiology
EH ethnology ET etiology
GE genetics HI history
IM immunology ME metabolism
MI microbiology MO mortality
NU nursing PS parasitology
PA pathology PP physiopathology
PC prevention & control PX psychology
RT radiotherapy RH rehabilitation
SU surgery TH therapy
UR urine VE veterinary
VI virology  
Record Number:   53517 
Unique Identifier:   D057177 

Occurrence in VHL:
 

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