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...
Spremljeno u:
| Glavni autori: | , |
|---|---|
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Springer
2024-07-01
|
| Serija: | Journal of Rare Diseases |
| Teme: | |
| Online pristup: | https://doi.org/10.1007/s44162-024-00039-w |
| Oznake: |
Bez oznaka, Budi prvi tko označuje ovaj zapis!
|