A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Facial trichilemmomas and papillomatous papules of the oral mucosa are the most characteristic lesions. Individuals with this syndrome have a high risk of ; ; and . This syndrome is associated with mutations in the gene for .
Doença de Cowden /
Síndrome do Tumor Hamartoma PTEN /
Síndrome Bannayan-Riley-Ruvalcaba /
Síndrome do Hamartoma Tumoral PTEN /