| Display title | Medicine:Kapur–Toriello syndrome |
| Default sort key | Kapur-Toriello syndrome |
| Page length (in bytes) | 3,185 |
| Namespace ID | 3048 |
| Namespace | Medicine |
| Page ID | 532997 |
| 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>John Stpola |
| Date of page creation | 15:28, 2 November 2022 |
| Latest editor | imported>John Stpola |
| Date of latest edit | 15:28, 2 November 2022 |
| 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. | Kapur–Toriello syndrome is a rare autosomal recessive genetic disorder. The defining feature of Kapur–Toriello syndrome is abnormal morphology of the columella, the end of the nasal septum, which in the syndrome extends below the margin of the nostrils. |
