Hoseini B

ORCID: 0000-0002-0355-6181 · 1 paper in corpus

2023

PTEN hamartoma tumour syndrome: case report based on data from the Iranian hereditary colorectal cancer registry and literature review.

Diagnostic pathology ·doi:10.1186/s13000-023-01331-x

BackgroundPTEN hamartoma tumour syndrome (PHTS) is a rare hereditary disorder caused by germline pathogenic mutations in the PTEN gene. This study presents a case of PHTS referred for genetic evaluation due to multiple polyps in the rectosi…