Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the <i>PTEN</i> hamartoma tumour syndrome: Table 1

Abstract excerpt

PTEN hamartoma tumour syndrome Since consensus operational diagnostic criteria for Cowden syndrome (MIM 158350) were first established in 1995, our understanding of this complex disease—and the spectrum of disorders related to it by virtue of also having germline mutations in the PTEN tumour suppressor gene—has continued to evolve. This was reflected in a commentary1 in this journal in 2000 in which it was...

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