Difference between revisions of "Neurodegenerative diseases"

Jump to navigation Jump to search
→‎Overview: FUSopathies added
(+pictures for DLB)
(→‎Overview: FUSopathies added)
Line 12: Line 12:
{{familytree/start}}                       
{{familytree/start}}                       
{{familytree  | | | | | | | A01 | | | | | | | | A01=Neurodegenerative<br>disorders}}
{{familytree  | | | | | | | A01 | | | | | | | | A01=Neurodegenerative<br>disorders}}
{{familytree  | |,|-|-|-|v|-|^|-|v|-|-|-|.| | |}}
{{familytree  | |,|-|-|-|v|-|^|-|v|-|-|-|v|-|-|-|.| | |}}
{{familytree  | B01 | | B02 | | B03 | | B04 | |B01=Amyloidoses|B02=Tauopathies|B03=α-synucleinopathies|B04=TDP-43}}
{{familytree  | B01 | | B02 | | B03 | | B04 | | B05 || B01=Amyloidoses|B02=Tauopathies|B03=α-synucleinopathies|B04=TDP-43|B05=FUS}}
{{familytree/end}}
{{familytree/end}}


Line 37: Line 37:


FUS proteinopathies:
FUS proteinopathies:
*[[Amyotrophic lateral sclerosis]].
*Basophilic inclusion body disease (BIBD).
*Frontotemporal lobar degeneration.
*Neuronal intermediate filament inclusion disease (NIFID).
*Frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD-U).


Prionopathies:
Prionopathies:
Account-creators
1,040

edits

Navigation menu