Difference between revisions of "Neurodegenerative diseases"

Jump to navigation Jump to search
→‎Overview: table, disease, clinical
m (overview)
(→‎Overview: table, disease, clinical)
Line 10: Line 10:
{{familytree  | B01 | | B02 | | B03 | | B04 | |B01=Amyloidoses|B02=Tauopathies|B03=α-synucleinopathies|B04=TDP-43}}
{{familytree  | B01 | | B02 | | B03 | | B04 | |B01=Amyloidoses|B02=Tauopathies|B03=α-synucleinopathies|B04=TDP-43}}
{{familytree/end}}
{{familytree/end}}
===Common diseases===
[[Amyloid]]oses:
*Alzheimer disease (Abeta).
*Creutzfeldt-Jakob disease (PrP).
Taupathies:
*Progressive supranuclear palsy.
*Pick's disease.
Synucleinopathies:
*Parkinson disease.
*Dementia with Lewy bodies.
*Multiple system atrophy.
TDP-43 proteinopathies:
*Amyotrophic alteral sclerosis.
*Frontotemporal lobar degeneration with ubiquitinated inclusions.
====Table===
Disease/pathology/clinical correlation based on ''Dickson'':<ref name=pmid19918325>{{cite journal |author=Dickson DW |title=Neuropathology of non-Alzheimer degenerative disorders |journal=Int J Clin Exp Pathol |volume=3 |issue=1 |pages=1–23 |year=2009 |pmid=19918325 |pmc=2776269 |doi= |url=http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2776269/?tool=pubmed}}</ref>
{| class="wikitable sortable" style="margin-left:auto;margin-right:auto"
| '''Disease'''
| '''Mutated protein'''
| '''Distribution'''
| '''Clinical'''
| '''Image'''
|-
| Alzheimer disease
| Abeta (mutated ''APP'')
| corticolimbic
| dementia
| Image?
|-
| Creutzfeldt-Jakob disease
| PrP<sup>res</sup>
| cortical & basal ganglia
| rapid progression dementia, <br>movement disorder
| Image?
|-
| Progressive supranuclear palsy
| tau 4R
| basal ganglia, brainstem
| parkinsonism
| Image?
|-
| Pick disease
| tau 3R
| corticolimbic
| dementia + focal <br>cortical syndrome
| Image?
|-
| Parkinson disease
| alpha-synuclein
| brainstem
| parkinsonism
| Image?
|-
| Dementia with Lewy bodies
| alpha-synuclein
| corticolimbic, brainstem
| dementia + parkinsonism
| Image?
|-
| Multiple system atrophy
| alpha-synuclein
| basal ganglia, brainstem, cerebellum
| ataxia, parkinsonism
| Image
|-
| Amyotrophic lateral sclerosis
| TDP-43
| motor neurons
| spasticity, weakness
| Image
|-
| Frontotemporal lobar degeneration with ubiquitinated inclusions
| TDP-43
| cortex, basal ganglia
| dementia, focal cortical syndromes
| Image?
|- <!--
| Disease
| Mutated protein
| Distribution
| Clinical
| Image -->
|}
==IHC==
*AT-8 = stains phosphorylated tau.<ref name=pmid19946779>{{cite journal |author=Seelaar H, Klijnsma KY, de Koning I, ''et al.'' |title=Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration |journal=J. Neurol. |volume=257 |issue=5 |pages=747–53 |year=2010 |month=May |pmid=19946779 |pmc=2864899 |doi=10.1007/s00415-009-5404-z |url=http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2864899/}}</ref>
*p62; poli-ubiquitin-binding protein p62.<ref name=pmid19946779/>
*TDP-43.


==General DDx of dementia==
==General DDx of dementia==
48,470

edits

Navigation menu