Cowden's disease or multiple hamartoma syndrome is an autosomal dominant inherited disease and the main dermatological features are facial trichilemmomas (hamartomas of the follicular infundibula), oral fibroma and benign acral keratoses. The importance of this disease lays in the increased susceptibility to malignization of some lesions, especially breast, thyroid and genitourinary tract. Despite its varied phenotypic expression, this disease is generally unknown. Consequently, many cases are undiagnosed or diagnosis comes at a late stage, which reinforces the importance of an early investigation of the disease so the patient may have periodic check-ups to discover and treat malignancies
A síndrome de Cowden (SC) ou síndrome de múltiplos hamartomas (SMH) é genodermatose rara de herança ...
Cowden syndrome is a rare genodermatosis of autosomal dominant inheritance characterized by multiple...
Cowden's disease, or multiple hamartoma syndrome, is an uncommon condition with characteristic mucoc...
Copyright © 2013 Prashanthi Chippagiri et al. This is an open access article distributed under the C...
PubMed ID: 10540825First lesions of Cowden syndrome appear in the oral cavity and on the skin. Malig...
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...
Cowden?s disease, or multiple hamartoma syndrome, is an autosomal dominant genodermatosis, character...
Cowden syndrome (CS; also known as multiple hamartoma syndrome) is a rare autosomal dominant disorde...
Os autores descrevem um caso de doença de Cowden ou síndrome dos hamartomas múltiplos. Doença de tra...
Cowden's disease, or multiple hamartoma syndrome, is a rare condition classified recently as a hered...
A typical case of Cowden disease is presented. This is rare mucocutaneous disease, genetically deter...
Cowden syndrome (CS) is an autosomal dominant disorder characterized by presence of multiple hamarto...
BACKGROUND: Cowden syndrome is an autosomal-dominant hereditary cancer syndrome with high variabilit...
An analysis of the findings in 21 patients with the Cowden syndrome or the multiple hamartoma syndro...
A síndrome de Cowden (SC) ou síndrome de múltiplos hamartomas (SMH) é genodermatose rara de herança ...
Cowden syndrome is a rare genodermatosis of autosomal dominant inheritance characterized by multiple...
Cowden's disease, or multiple hamartoma syndrome, is an uncommon condition with characteristic mucoc...
Copyright © 2013 Prashanthi Chippagiri et al. This is an open access article distributed under the C...
PubMed ID: 10540825First lesions of Cowden syndrome appear in the oral cavity and on the skin. Malig...
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...
Cowden?s disease, or multiple hamartoma syndrome, is an autosomal dominant genodermatosis, character...
Cowden syndrome (CS; also known as multiple hamartoma syndrome) is a rare autosomal dominant disorde...
Os autores descrevem um caso de doença de Cowden ou síndrome dos hamartomas múltiplos. Doença de tra...
Cowden's disease, or multiple hamartoma syndrome, is a rare condition classified recently as a hered...
A typical case of Cowden disease is presented. This is rare mucocutaneous disease, genetically deter...
Cowden syndrome (CS) is an autosomal dominant disorder characterized by presence of multiple hamarto...
BACKGROUND: Cowden syndrome is an autosomal-dominant hereditary cancer syndrome with high variabilit...
An analysis of the findings in 21 patients with the Cowden syndrome or the multiple hamartoma syndro...
A síndrome de Cowden (SC) ou síndrome de múltiplos hamartomas (SMH) é genodermatose rara de herança ...
Cowden syndrome is a rare genodermatosis of autosomal dominant inheritance characterized by multiple...
Cowden's disease, or multiple hamartoma syndrome, is an uncommon condition with characteristic mucoc...