Copyright © 2013 Prashanthi Chippagiri et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Aim. To present a case of Cowden’s syndrome and emphasize the importance of continued cancer surveillance in these patients. Cowden syndrome is an inherited autosomal dominant trait with incomplete penetrance and a range of expressivity. It is characterized by multiple hamartomas and neoplasms. Mucocutaneous features include trichilemmomas, oral mucosal papillomatosis, acral keratosis, and palmoplantar keratosis. Here, we report a case of Cowdens syndrome of a 30-year-old female patie...
An analysis of the findings in 21 patients with the Cowden syndrome or the multiple hamartoma syndro...
Cowden's disease, or multiple hamartoma syndrome, is a rare condition classified recently as a hered...
Cowden syndrome (CS) is an autosomal dominant genodermatosis that frequently affects several tissues...
Cowden syndrome or multiple hamartoma syndrome is an autosomal dominant condition with variable expr...
Cowden syndrome (CS; also known as multiple hamartoma syndrome) is a rare autosomal dominant disorde...
Cowden's disease or multiple hamartoma syndrome is an autosomal dominant inherited disease and the m...
BACKGROUND: Cowden syndrome is an autosomal-dominant hereditary cancer syndrome with high variabilit...
Cowden?s disease, or multiple hamartoma syndrome, is an autosomal dominant genodermatosis, character...
Cowden syndrome is a rare autosomal dominant familial cancer syndrome with a high risk of breast can...
Cowden syndrome is an autosomal dominant rare inherited disorder characterized by multiple hamartoma...
Os autores descrevem um caso de doença de Cowden ou síndrome dos hamartomas múltiplos. Doença de tra...
Cowden's syndrome is an autosomal dominant genodermatosis with variable orofacial and systemic manif...
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...
Cowden's disease, or multiple hamartoma syndrome, is an uncommon condition with characteristic mucoc...
An analysis of the findings in 21 patients with the Cowden syndrome or the multiple hamartoma syndro...
Cowden's disease, or multiple hamartoma syndrome, is a rare condition classified recently as a hered...
Cowden syndrome (CS) is an autosomal dominant genodermatosis that frequently affects several tissues...
Cowden syndrome or multiple hamartoma syndrome is an autosomal dominant condition with variable expr...
Cowden syndrome (CS; also known as multiple hamartoma syndrome) is a rare autosomal dominant disorde...
Cowden's disease or multiple hamartoma syndrome is an autosomal dominant inherited disease and the m...
BACKGROUND: Cowden syndrome is an autosomal-dominant hereditary cancer syndrome with high variabilit...
Cowden?s disease, or multiple hamartoma syndrome, is an autosomal dominant genodermatosis, character...
Cowden syndrome is a rare autosomal dominant familial cancer syndrome with a high risk of breast can...
Cowden syndrome is an autosomal dominant rare inherited disorder characterized by multiple hamartoma...
Os autores descrevem um caso de doença de Cowden ou síndrome dos hamartomas múltiplos. Doença de tra...
Cowden's syndrome is an autosomal dominant genodermatosis with variable orofacial and systemic manif...
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...
Cowden's disease, or multiple hamartoma syndrome, is an uncommon condition with characteristic mucoc...
An analysis of the findings in 21 patients with the Cowden syndrome or the multiple hamartoma syndro...
Cowden's disease, or multiple hamartoma syndrome, is a rare condition classified recently as a hered...
Cowden syndrome (CS) is an autosomal dominant genodermatosis that frequently affects several tissues...