Add to ORKGCowden?s disease, or multiple hamartoma syndrome, is an autosomal dominant genodermatosis, characterized by the presence of multiple cutaneous hamartomas, oral fibromas and benign acral keratosis. It affects multiple organs (breast, thyroids, stomach, colon), with the strong possibility of malignant neoplasia developing in these organs. We present a case of this rare syndrome, highlighting the presentation of some clinical characteristics that, in suspected cases, can help to establish an early diagnosis of this disease, this being of great importance given the high frequency of tumors in people with this clinical picture
Cowden syndrome is a rare autosomal dominant familial cancer syndrome with a high risk of breast can...
Cowdenâ s Syndrome (CS) is a rare congenital autosomal dominant disorder that affects around 1/2000...
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 autosomal dominant genodermatosis, character...
Cowden syndrome (CS) is an autosomal dominant genodermatosis that frequently affects several tissues...
Copyright © 2013 Prashanthi Chippagiri et al. This is an open access article distributed under the C...
Introdução: A síndrome de Cowden é um distúrbio multissistêmico de predisposição a diversos tipos de...
El síndrome de Cowden es una infrecuente enfermedad hereditaria englobada dentro de las poliposis ga...
A síndrome de Cowden (SC) ou síndrome de múltiplos hamartomas (SMH) é genodermatose rara de herança ...
Os autores descrevem um caso de doença de Cowden ou síndrome dos hamartomas múltiplos. Doença de tra...
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 syndrome or multiple hamartoma syndrome is an autosomal dominant condition with variable expr...
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 is a rare autosomal dominant familial cancer syndrome with a high risk of breast can...
Cowdenâ s Syndrome (CS) is a rare congenital autosomal dominant disorder that affects around 1/2000...
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 autosomal dominant genodermatosis, character...
Cowden syndrome (CS) is an autosomal dominant genodermatosis that frequently affects several tissues...
Copyright © 2013 Prashanthi Chippagiri et al. This is an open access article distributed under the C...
Introdução: A síndrome de Cowden é um distúrbio multissistêmico de predisposição a diversos tipos de...
El síndrome de Cowden es una infrecuente enfermedad hereditaria englobada dentro de las poliposis ga...
A síndrome de Cowden (SC) ou síndrome de múltiplos hamartomas (SMH) é genodermatose rara de herança ...
Os autores descrevem um caso de doença de Cowden ou síndrome dos hamartomas múltiplos. Doença de tra...
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 syndrome or multiple hamartoma syndrome is an autosomal dominant condition with variable expr...
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 is a rare autosomal dominant familial cancer syndrome with a high risk of breast can...
Cowdenâ s Syndrome (CS) is a rare congenital autosomal dominant disorder that affects around 1/2000...
Cowden Syndrome (CS) was first described in 1963 by Lloyd and Dennis. It's an uncommon autosomal dom...