Peutz-Jeghers syndrome (Q46686): Difference between revisions
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Síndrome de Peutz-Jeghers (SPJ) é um transtorno hereditário autossômico dominante caracterizado por pólipos hamartomatosos intestinais em associação com um padrão distinto de deposição de melanina macular em pele e mucosa. Os pacientes têm um risco aumentado de desenvolver câncer intestinal. | |||
| description / en | description / en | ||
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. | |||
Revision as of 15:26, 13 August 2026
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 |
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| 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. |
