Cowden syndrome (CS) is an autosomal dominant genodermatosis that frequently affects several tissues with hamartomatous growth. The oral cavity is quite commonly involved with papillomatous lesions, which can be crucial to early diagnosis of this disease. In this series, 10 patients with a great diversity of manifestations associated with CS are presented, in whom oral papillomatosis was a constant and relevant finding to establish the diagnosis of CS. The role of the dentist in recognizing the oral lesions, the other diagnostic criteria, the risk for the development of malignancies, and the importance of lifetime follow-up are discussed.Cowden syndrome (CS) is an autosomal dominant genodermatosis that frequently affects several tissues wit...
Cowden's syndrome is an autosomal dominant genodermatosis with variable orofacial and systemic manif...
Cowden syndrome is a rare genodermatosis of autosomal dominant inheritance characterized by multiple...
BACKGROUND: Phosphatase and tensin homolog (PTEN) hamartoma tumor syndrome (PHTS) encompasses sever...
Cowden?s disease, or multiple hamartoma syndrome, is an autosomal dominant genodermatosis, character...
BACKGROUND: Cowden syndrome is an autosomal-dominant hereditary cancer syndrome with high variabilit...
Cowden syndrome or multiple hamartoma syndrome is an autosomal dominant condition with variable expr...
PubMed ID: 10540825First lesions of Cowden syndrome appear in the oral cavity and on the skin. Malig...
Aim. Cowden’s Syndrome (CS) is an autosomal dominant disorder associated with mutations in PTEN (Pho...
Introdução: A síndrome de Cowden é um distúrbio multissistêmico de predisposição a diversos tipos de...
Copyright © 2013 Prashanthi Chippagiri et al. This is an open access article distributed under the C...
Cowdenâ s Syndrome (CS) is a rare congenital autosomal dominant disorder that affects around 1/2000...
A typical case of Cowden disease is presented. This is rare mucocutaneous disease, genetically deter...
Cowden Syndrome (CS) was first described in 1963 by Lloyd and Dennis. It's an uncommon autosomal dom...
Cowden's Syndrome (CS) is a rare congenital autosomal dominant disorder that affects around 1/200000...
An analysis of the findings in 21 patients with the Cowden syndrome or the multiple hamartoma syndro...
Cowden's syndrome is an autosomal dominant genodermatosis with variable orofacial and systemic manif...
Cowden syndrome is a rare genodermatosis of autosomal dominant inheritance characterized by multiple...
BACKGROUND: Phosphatase and tensin homolog (PTEN) hamartoma tumor syndrome (PHTS) encompasses sever...
Cowden?s disease, or multiple hamartoma syndrome, is an autosomal dominant genodermatosis, character...
BACKGROUND: Cowden syndrome is an autosomal-dominant hereditary cancer syndrome with high variabilit...
Cowden syndrome or multiple hamartoma syndrome is an autosomal dominant condition with variable expr...
PubMed ID: 10540825First lesions of Cowden syndrome appear in the oral cavity and on the skin. Malig...
Aim. Cowden’s Syndrome (CS) is an autosomal dominant disorder associated with mutations in PTEN (Pho...
Introdução: A síndrome de Cowden é um distúrbio multissistêmico de predisposição a diversos tipos de...
Copyright © 2013 Prashanthi Chippagiri et al. This is an open access article distributed under the C...
Cowdenâ s Syndrome (CS) is a rare congenital autosomal dominant disorder that affects around 1/2000...
A typical case of Cowden disease is presented. This is rare mucocutaneous disease, genetically deter...
Cowden Syndrome (CS) was first described in 1963 by Lloyd and Dennis. It's an uncommon autosomal dom...
Cowden's Syndrome (CS) is a rare congenital autosomal dominant disorder that affects around 1/200000...
An analysis of the findings in 21 patients with the Cowden syndrome or the multiple hamartoma syndro...
Cowden's syndrome is an autosomal dominant genodermatosis with variable orofacial and systemic manif...
Cowden syndrome is a rare genodermatosis of autosomal dominant inheritance characterized by multiple...
BACKGROUND: Phosphatase and tensin homolog (PTEN) hamartoma tumor syndrome (PHTS) encompasses sever...