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Germline PTEN/MMAC1/TEP1 mutations and association with gastrointestinal manifestations in Cowden disease

✍ Scribed by Weber, H.C.; Marsh, D.; Lubensky, I.; Lin, A.; Eng, C.

Book ID
122125884
Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
172 KB
Volume
114
Category
Article
ISSN
0016-5085

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✍ Debbie J. Marsh; Patricia L. M. Dahia; ValΓ©rie Coulon; Zimu Zheng; FranΓ§oise Dor πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 174 KB πŸ‘ 3 views

Cowden disease (CD) is a rare, autosomal dominant inherited cancer syndrome characterized by multiple benign and malignant lesions in a wide spectrum of tissues. While individuals with CD have an increased risk of breast and thyroid neoplasms, the primary features of CD are hamartomas. The gene for