| Display title | Medicine:Progressive familial intrahepatic cholestasis |
| Default sort key | Progressive familial intrahepatic cholestasis |
| Page length (in bytes) | 9,836 |
| Namespace ID | 3048 |
| Namespace | Medicine |
| Page ID | 870111 |
| 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>Unex |
| Date of page creation | 03:16, 5 February 2024 |
| Latest editor | imported>Unex |
| Date of latest edit | 03:16, 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. | Progressive familial intrahepatic cholestasis (PFIC) is a group of familial cholestatic conditions caused by defects in biliary epithelial transporters. The clinical presentation usually occurs first in childhood with progressive cholestasis. This usually leads to failure to thrive, cirrhosis, and the... |
