| Display title | Medicine:Mohr–Tranebjærg syndrome |
| Default sort key | Mohr-Tranebjaerg syndrome |
| Page length (in bytes) | 9,576 |
| Namespace ID | 3048 |
| Namespace | Medicine |
| Page ID | 2232184 |
| 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>Smart bot editor |
| Date of page creation | 00:25, 5 February 2024 |
| Latest editor | imported>Smart bot editor |
| Date of latest edit | 00:25, 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. | Mohr–Tranebjærg syndrome (MTS) is a rare X-linked recessive syndrome also known as deafness–dystonia syndrome and caused by mutation in the TIMM8A gene. It is characterized by clinical manifestations commencing with early childhood onset hearing loss, followed by adolescent onset progressive dystonia... |
