Cowden's syndrome is an autosomal dominant genodermatosis with variable orofacial and systemic manifestations. Here we present one such classical case of Cowden's syndrome in a 45-year-old female patient with features such as multiple cutaneous papillomatosis, oral fibromas, and fibromas involving multiple organs such as gastrointestinal tract (multiple polyps), thyroid disorders, and breast cancer
Cowden's disease or multiple hamartoma syndrome is an autosomal dominant inherited disease and the m...
Abstract Background Cowden syndrome (CS) is a cancer predisposition syndrome associated with increas...
Cowden syndrome (CS) is a genetic cancerpredisposition syndrome that is associated withgermline muta...
Cowden syndrome or multiple hamartoma syndrome is an autosomal dominant condition with variable expr...
Cowden syndrome is an autosomal dominant rare inherited disorder characterized by multiple hamartoma...
Copyright © 2013 Prashanthi Chippagiri et al. This is an open access article distributed under the C...
Cowden syndrome (CS; also known as multiple hamartoma syndrome) is a rare autosomal dominant disorde...
Cowden syndrome is a rare genodermatosis of autosomal dominant inheritance characterized by multiple...
An analysis of the findings in 21 patients with the Cowden syndrome or the multiple hamartoma syndro...
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 (CS) is an autosomal dominant genodermatosis that frequently affects several tissues...
Cowden syndrome is a rare autosomal dominant familial cancer syndrome with a high risk of breast can...
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's disease or multiple hamartoma syndrome is an autosomal dominant inherited disease and the m...
Abstract Background Cowden syndrome (CS) is a cancer predisposition syndrome associated with increas...
Cowden syndrome (CS) is a genetic cancerpredisposition syndrome that is associated withgermline muta...
Cowden syndrome or multiple hamartoma syndrome is an autosomal dominant condition with variable expr...
Cowden syndrome is an autosomal dominant rare inherited disorder characterized by multiple hamartoma...
Copyright © 2013 Prashanthi Chippagiri et al. This is an open access article distributed under the C...
Cowden syndrome (CS; also known as multiple hamartoma syndrome) is a rare autosomal dominant disorde...
Cowden syndrome is a rare genodermatosis of autosomal dominant inheritance characterized by multiple...
An analysis of the findings in 21 patients with the Cowden syndrome or the multiple hamartoma syndro...
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 (CS) is an autosomal dominant genodermatosis that frequently affects several tissues...
Cowden syndrome is a rare autosomal dominant familial cancer syndrome with a high risk of breast can...
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's disease or multiple hamartoma syndrome is an autosomal dominant inherited disease and the m...
Abstract Background Cowden syndrome (CS) is a cancer predisposition syndrome associated with increas...
Cowden syndrome (CS) is a genetic cancerpredisposition syndrome that is associated withgermline muta...