Peutz-Jeghers syndrome (Q46686): Difference between revisions
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Revision as of 15:27, 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 |
||
| 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. |
Statements
CID11:LD2D.0
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dki-india-LD2D.0
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Concluído
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13 August 2026
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