| Display title | Medicine:McCune–Albright syndrome |
| Default sort key | McCune-Albright syndrome |
| Page length (in bytes) | 22,428 |
| Namespace ID | 3048 |
| Namespace | Medicine |
| Page ID | 865013 |
| 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>DanMescoff |
| Date of page creation | 01:58, 5 February 2024 |
| Latest editor | imported>DanMescoff |
| Date of latest edit | 01:58, 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. | McCune–Albright syndrome is a complex genetic disorder affecting the bone, skin and endocrine systems. It is a mosaic disease arising from somatic activating mutations in GNAS, which encodes the alpha-subunit of the Gs heterotrimeric G protein.
It was first described in 1937 by American pediatrician... |
