| Display title | Medicine:Andersen–Tawil syndrome |
| Default sort key | Andersen-Tawil syndrome |
| Page length (in bytes) | 24,635 |
| Namespace ID | 3048 |
| Namespace | Medicine |
| Page ID | 1008395 |
| 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>Wikisleeper |
| Date of page creation | 09:53, 14 February 2024 |
| Latest editor | imported>Wikisleeper |
| Date of latest edit | 09:53, 14 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. | Andersen–Tawil syndrome, also called Andersen syndrome and long QT syndrome 7, is a rare genetic disorder affecting several parts of the body. The three predominant features of Andersen–Tawil syndrome include disturbances of the electrical function of the heart characterised by an abnormality seen on... |
