Cowden syndrome: Familial presentation and genetic insights
Cowden syndrome (CS), primarily driven by PTEN gene mutations, leads to aberrant cell proliferation and presents with characteristic manifestations including multiple hematomas, hamartomatous polyps, and trichilemmomas. Beyond these, patients face elevated risks of breast, thyroid, and endometrial t...
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Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2024-12-01
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Series: | Indian Journal of Community and Family Medicine |
Subjects: | |
Online Access: | https://journals.lww.com/10.4103/ijcfm.ijcfm_94_23 |
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