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Constitutional Mutation of PIK3CA: A Variant of Cowden Syndrome?
1. Introduction Cowden syndrome (CS), also known as PTEN hamartoma tumor syndrome, increases the risk for benign and malignant tumors of the thyroid, breast, kidney, and endometrium. Consensus clinical diagnostic criteria for CS [1] and a scoring system based on the phenotype and age at diagnosis of CS [2] have been developed in order to identify PTEN germline mutations.
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