Add to ORKGCowden syndrome (CS) is a genetic cancerpredisposition syndrome that is associated withgermline mutations in the phosphate and tensinhomologue deleted on chromosome ten (PTEN)tumor suppressor gene. It is characterizedby the formation of benign and malignanttumors. Characteristic benign tumors includetrichilemmommas, acral keratoses, mucocutaneousneuromas, and oral papillomas. The most commonmalignant condition include breast, thyroid, andendometrial cancers. We present a case of a30-year-old woman with CS, who initially presentedwith trichilemmomas that were misdiagnosed ascomedonal acne. Recognition of the presentingfeatures of CS is important to ensure proper referral,management, and treatment for these patients
A 47-year-old woman, initially diagnosed in 1996 with Cowden syndrome (CS), PTEN-mutant bilateral br...
Copyright © 2013 Prashanthi Chippagiri et al. This is an open access article distributed under the C...
An analysis of the findings in 21 patients with the Cowden syndrome or the multiple hamartoma syndro...
Cowden syndrome (CS) is a genetic cancerpredisposition syndrome that is associated withgermline muta...
Cowden syndrome (CS; also known as multiple hamartoma syndrome) is a rare autosomal dominant disorde...
Cowden syndrome or multiple hamartoma syndrome is an autosomal dominant condition with variable expr...
Abstract Background Cowden syndrome (CS) is a cancer predisposition syndrome associated with increas...
Cowden syndrome (CS) is an autosomal dominant disorder characterized by presence of multiple hamarto...
Cowden syndrome is a rare genodermatosis of autosomal dominant inheritance characterized by multiple...
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...
Cowden syndrome (CS) is an infrequent genodermatosis caused by mutations in the phosphatase and tens...
Cowden syndrome (CS) is a phosphatase and tensin homolog gene (PTEN) -associated condition character...
Cowden disease (CD) is characterised by multiple hamartomas in a variety of tissues. The pathologica...
A 47-year-old woman, initially diagnosed in 1996 with Cowden syndrome (CS), PTEN-mutant bilateral br...
Copyright © 2013 Prashanthi Chippagiri et al. This is an open access article distributed under the C...
An analysis of the findings in 21 patients with the Cowden syndrome or the multiple hamartoma syndro...
Cowden syndrome (CS) is a genetic cancerpredisposition syndrome that is associated withgermline muta...
Cowden syndrome (CS; also known as multiple hamartoma syndrome) is a rare autosomal dominant disorde...
Cowden syndrome or multiple hamartoma syndrome is an autosomal dominant condition with variable expr...
Abstract Background Cowden syndrome (CS) is a cancer predisposition syndrome associated with increas...
Cowden syndrome (CS) is an autosomal dominant disorder characterized by presence of multiple hamarto...
Cowden syndrome is a rare genodermatosis of autosomal dominant inheritance characterized by multiple...
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...
Cowden syndrome (CS) is an infrequent genodermatosis caused by mutations in the phosphatase and tens...
Cowden syndrome (CS) is a phosphatase and tensin homolog gene (PTEN) -associated condition character...
Cowden disease (CD) is characterised by multiple hamartomas in a variety of tissues. The pathologica...
A 47-year-old woman, initially diagnosed in 1996 with Cowden syndrome (CS), PTEN-mutant bilateral br...
Copyright © 2013 Prashanthi Chippagiri et al. This is an open access article distributed under the C...
An analysis of the findings in 21 patients with the Cowden syndrome or the multiple hamartoma syndro...