A rare case report of the Cowden syndrome
Abstract Cowden syndrome (CS) is a rare autosomal dominant genodermatosis caused by a heterozygous germline mutation in the PTEN gene, found in nearly 80% of cases. It is characterized by multiple benign hamartomas which manifest across various organs. This condition is further distinguished by its...
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| Hauptverfasser: | , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Springer
2024-07-01
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| Schriftenreihe: | Journal of Rare Diseases |
| Schlagworte: | |
| Online-Zugang: | https://doi.org/10.1007/s44162-024-00039-w |
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