Thyroid pathology, a clue to PTEN hamartoma tumor syndrome
Phosphatase and tensin homolog (PTEN) hamartoma tumor syndrome (PHTS) is a hereditary disorder caused by germline inactivating mutations in the PTEN tumor suppressor gene. As a type of PHTS, Cowden syndrome is associated with abnormalities of the thyroid, breast, uterus, and gastrointestinal tract....
| Autors principals: | , |
|---|---|
| Format: | Article |
| Idioma: | English |
| Publicat: |
Korean Society of Pathologists & the Korean Society for Cytopathology
2023-05-01
|
| Col·lecció: | Journal of Pathology and Translational Medicine |
| Matèries: | |
| Accés en línia: | http://jpatholtm.org/upload/pdf/jptm-2023-03-04.pdf |