Add to ORKGA typical case of Cowden disease is presented. This is rare mucocutaneous disease, genetically determined, with multiple organ system involvement in which a malignancy, particularly of breast and thyroid gland, may develop. The disease can be diagnosed in its early stages by gingival and cutaneous manifestations. We emphasize that the dentist may be the first health care professional who recognizes the syndrome, which is a crucial step to prevent and cure the predictable malignancy
Cowden syndrome (CS) is an autosomal dominant disorder characterized by presence of multiple hamarto...
An analysis of the findings in 21 patients with the Cowden syndrome or the multiple hamartoma syndro...
Cowden syndrome (CS; also known as multiple hamartoma syndrome) is a rare autosomal dominant disorde...
A typical case of Cowden disease is presented. This is rare mucocutaneous disease, genetically deter...
PubMed ID: 10540825First lesions of Cowden syndrome appear in the oral cavity and on the skin. Malig...
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 syndrome (CS) is an autosomal dominant genodermatosis that frequently affects several tissues...
Cowden?s disease, or multiple hamartoma syndrome, is an autosomal dominant genodermatosis, character...
Copyright © 2013 Prashanthi Chippagiri et al. This is an open access article distributed under the C...
Aim. Cowden’s Syndrome (CS) is an autosomal dominant disorder associated with mutations in PTEN (Pho...
Cowden Syndrome (CS) was first described in 1963 by Lloyd and Dennis. It's an uncommon autosomal dom...
Cowden's disease, or multiple hamartoma syndrome, is an uncommon condition with characteristic mucoc...
Cowden's disease, or multiple hamartoma syndrome, is a rare condition classified recently as a hered...
Cowden syndrome or multiple hamartoma syndrome is an autosomal dominant condition with variable expr...
Cowden syndrome (CS) is an autosomal dominant disorder characterized by presence of multiple hamarto...
An analysis of the findings in 21 patients with the Cowden syndrome or the multiple hamartoma syndro...
Cowden syndrome (CS; also known as multiple hamartoma syndrome) is a rare autosomal dominant disorde...
A typical case of Cowden disease is presented. This is rare mucocutaneous disease, genetically deter...
PubMed ID: 10540825First lesions of Cowden syndrome appear in the oral cavity and on the skin. Malig...
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 syndrome (CS) is an autosomal dominant genodermatosis that frequently affects several tissues...
Cowden?s disease, or multiple hamartoma syndrome, is an autosomal dominant genodermatosis, character...
Copyright © 2013 Prashanthi Chippagiri et al. This is an open access article distributed under the C...
Aim. Cowden’s Syndrome (CS) is an autosomal dominant disorder associated with mutations in PTEN (Pho...
Cowden Syndrome (CS) was first described in 1963 by Lloyd and Dennis. It's an uncommon autosomal dom...
Cowden's disease, or multiple hamartoma syndrome, is an uncommon condition with characteristic mucoc...
Cowden's disease, or multiple hamartoma syndrome, is a rare condition classified recently as a hered...
Cowden syndrome or multiple hamartoma syndrome is an autosomal dominant condition with variable expr...
Cowden syndrome (CS) is an autosomal dominant disorder characterized by presence of multiple hamarto...
An analysis of the findings in 21 patients with the Cowden syndrome or the multiple hamartoma syndro...
Cowden syndrome (CS; also known as multiple hamartoma syndrome) is a rare autosomal dominant disorde...