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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....
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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The Korean Society of Pathologists and the Korean Society for Cytopathology
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10209666/ https://www.ncbi.nlm.nih.gov/pubmed/36977604 http://dx.doi.org/10.4132/jptm.2023.03.04 |