| Display title | Medicine:X-linked complicated corpus callosum dysgenesis |
| Default sort key | X-linked complicated corpus callosum dysgenesis |
| Page length (in bytes) | 8,053 |
| Namespace ID | 3048 |
| Namespace | Medicine |
| Page ID | 2220587 |
| 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>Jport |
| Date of page creation | 00:30, 5 February 2024 |
| Latest editor | imported>Jport |
| Date of latest edit | 00:30, 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. | X-linked complicated corpus callosum dysgenesis is a genetic disorder characterized by dysplasia, hypoplasia or agenesis of the corpus callosum alongside variable intellectual disability and spastic paraplegia. Only 13 cases (all male) have been described in medical literature. Transmission is X-linked... |
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