| Display title | Medicine:Occipital horn syndrome |
| Default sort key | Occipital horn syndrome |
| Page length (in bytes) | 12,945 |
| Namespace ID | 3048 |
| Namespace | Medicine |
| Page ID | 917868 |
| 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>HamTop |
| Date of page creation | 22:16, 7 February 2024 |
| Latest editor | imported>HamTop |
| Date of latest edit | 22:16, 7 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. | Occipital horn syndrome (OHS), formerly considered a variant of Ehlers–Danlos syndrome, is an X-linked recessive mitochondrial and connective tissue disorder. It is caused by a deficiency in the transport of the essential mineral copper, associated with mutations in the ATP7A gene.
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