Peutz-Jeghers syndrome (Q46686)
From determinar.ia.br - Determine suas informações
Peutz-Jeghers syndrome (PJS) is an autosomal dominant inherited disorder characterised by intestinal hamartomatous polyps in association with a distinct pattern of skin and mucosal macular melanin deposition. Patients have an increased risk of developing intestinal cancer.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD2D.0 |
||
| English | Peutz-Jeghers syndrome |
Peutz-Jeghers syndrome (PJS) is an autosomal dominant inherited disorder characterised by intestinal hamartomatous polyps in association with a distinct pattern of skin and mucosal macular melanin deposition. Patients have an increased risk of developing intestinal cancer. |
