| Display title | Medicine:Gerstmann–Sträussler–Scheinker syndrome |
| Default sort key | Gerstmann-Straussler-Scheinker syndrome |
| Page length (in bytes) | 13,631 |
| Namespace ID | 3048 |
| Namespace | Medicine |
| Page ID | 858043 |
| Page content language | en - English |
| Page content model | wikitext |
| Indexing by robots | Allowed |
| Number of redirects to this page | 0 |
| Counted as a content page | Yes |
| Page image |  |
| HandWiki item ID | None |
| Edit | Allow all users (infinite) |
| Move | Allow all users (infinite) |
| Page creator | imported>Wincert |
| Date of page creation | 01:22, 5 February 2024 |
| Latest editor | imported>Wincert |
| Date of latest edit | 01:22, 5 February 2024 |
| Total number of edits | 1 |
| Recent number of edits (within past 90 days) | 0 |
| Recent number of distinct authors | 0 |
Description | Content |
Article description: (description)
This attribute controls the content of the description and og:description elements. | Gerstmann–Sträussler–Scheinker syndrome (GSS) is an extremely rare, always fatal (due to it being caused by prions) neurodegenerative disease that affects patients from 20 to 60 years in age. It is exclusively heritable, and is found in only a few families all over the world. It is, however, classified... |
.jpg)
