| Display title | Medicine:Lesch–Nyhan syndrome |
| Default sort key | Lesch-Nyhan syndrome |
| Page length (in bytes) | 39,691 |
| Namespace ID | 3048 |
| Namespace | Medicine |
| Page ID | 860177 |
| 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>Pchauhan2001 |
| Date of page creation | 09:47, 14 February 2024 |
| Latest editor | imported>Pchauhan2001 |
| Date of latest edit | 09:47, 14 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. | Lesch–Nyhan syndrome (LNS) is a rare inherited disorder caused by a deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRT). This deficiency occurs due to mutations in the HPRT1 gene located on the X chromosome. LNS affects about 1 in 380,000 live births. The disorder was first... |
