User Tools

Site Tools


dementia

Differences

This shows you the differences between two versions of the page.

Link to this comparison view

Both sides previous revisionPrevious revision
dementia [2026/08/10 04:20] – [rapidly progressive dementia] gary1dementia [2026/08/10 04:22] (current) – [slowly progressive dementia] gary1
Line 77: Line 77:
   *[[fragileX|fragile X carriers]]   *[[fragileX|fragile X carriers]]
     *Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late onset neurodegenerative disorder associated with problems with movement (intentional tremor, Parkinsonism), memory, [[n_dysautonomia|dysautonomia]] and peripheral neuropathy. This is clinically different to Fragile X syndrome.     *Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late onset neurodegenerative disorder associated with problems with movement (intentional tremor, Parkinsonism), memory, [[n_dysautonomia|dysautonomia]] and peripheral neuropathy. This is clinically different to Fragile X syndrome.
-  *familial Alzheimer's disease +  *familial [[Alzheimers]] 
-  *other Alzheimer's disease+  *other [[Alzheimers]]
     * 80% heritability     * 80% heritability
     * two new genetic variants and 95 new gene interactions (epistasis) that may modulate the effects of variants in Alzheimer’s discovered by CSIRO in 2023     * two new genetic variants and 95 new gene interactions (epistasis) that may modulate the effects of variants in Alzheimer’s discovered by CSIRO in 2023
Line 91: Line 91:
   *pantothenate kinase-associated neurodegeneration   *pantothenate kinase-associated neurodegeneration
   *Tay-Sachs disease   *Tay-Sachs disease
-  *Wilson's disease+  *[[Wilsonsdisease]]
  
 ====environmental contributors==== ====environmental contributors====
dementia.txt · Last modified: 2026/08/10 04:22 by gary1

Donate Powered by PHP Valid HTML5 Valid CSS Driven by DokuWiki