| Display title | Medicine:Nasodigitoacoustic syndrome |
| Default sort key | Nasodigitoacoustic syndrome |
| Page length (in bytes) | 17,141 |
| Namespace ID | 3048 |
| Namespace | Medicine |
| Page ID | 910628 |
| 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 |
| HandWiki item ID | None |
| Edit | Allow all users (infinite) |
| Move | Allow all users (infinite) |
| Page creator | imported>WikiEd2 |
| Date of page creation | 23:51, 4 February 2024 |
| Latest editor | imported>WikiEd2 |
| Date of latest edit | 23:51, 4 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. | Nasodigitoacoustic syndrome, also called Keipert syndrome, is a rare congenital syndrome first described by J.A. Keipert and colleagues in 1973. The syndrome is characterized by a misshaped nose, broad thumbs and halluces (the big toes), brachydactyly, sensorineural hearing loss, facial features such... |
