| Display title | Medicine:Simpson–Golabi–Behmel syndrome |
| Default sort key | Simpson-Golabi-Behmel syndrome |
| Page length (in bytes) | 14,162 |
| Namespace ID | 3048 |
| Namespace | Medicine |
| Page ID | 916099 |
| 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>AIposter |
| Date of page creation | 01:17, 5 February 2024 |
| Latest editor | imported>AIposter |
| Date of latest edit | 01:17, 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. | Simpson–Golabi–Behmel syndrome (SGBS), is a rare inherited congenital disorder that can cause craniofacial, skeletal, vascular, cardiac, and renal abnormalities. There is a high prevalence of cancer associated in those with SGBS which includes wilms tumors, neuroblastoma, tumors of the adrenal gland... |
