Cowden syndrome is a risk factor for multiple neoplasm: a case report
Abstract Background Cowden’s syndrome is an autosomal dominant disease with variable penetrance, involving the tumor suppressor phosphatase and tension homolog gene, located on chromosome 10q22-23, responsible for cell proliferation, migration, and cellular apoptosis. Its clinical presentation encom...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2020-08-01
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Series: | World Journal of Surgical Oncology |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s12957-020-01971-z |