| Display title | Medicine:Incontinentia pigmenti |
| Default sort key | Incontinentia Pigmenti |
| Page length (in bytes) | 11,507 |
| Namespace ID | 3048 |
| Namespace | Medicine |
| Page ID | 865968 |
| 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>Jport |
| Date of page creation | 00:30, 5 February 2024 |
| Latest editor | imported>Jport |
| Date of latest edit | 00:30, 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. | Incontinentia pigmenti (IP) is a rare X-linked dominant genetic disorder that affects the skin, hair, teeth, nails and central nervous system. It is named from its appearance under a microscope.
The disease is characterized by skin abnormalities that begin in childhood, usually a blistering rash which... |
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