Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/339397
Type: Artigo
Title: Variable expressivity and novel PTEN mutations in Cowden syndrome
Author: Machado, Renato Assis
Ribeiro Paranaiba, Livia Maris
Martins, Luciane
Melo-Filho, Mario Rodrigues
de Souza, Thays Teixeira
Sayed Picciani, Bruna Lavinas
Silva-Junior, Geraldo Oliveira
Cantisano, Marilia Heffer
Rocha, Breno Amaral
Pires, Fabio Ramoa
Coletta, Ricardo D.
Abstract: Cowden syndrome (CS) is a phosphatase and tensin homolog gene (PTEN) -associated condition characterized by multiple mucocutaneous hamartomas and an increased risk of malignancies. We reported an isolated case and another of several individuals in one family affected by CS. The isolated case showed typical features, including fibrocystic breast disease, benign thyroid nodules, and multiple papillomatous lesions in the face and oral cavity, and the cause was a novel nonsense mutation-guanine (G) to thymine (T) transition at position 940 (c. 940 G>T)-in PTEN. In the family, the proband showed erythema nodosum, duodenal ulcer, intestinal polyps, cervical lipoma, renal cysts, and glaucoma, whereas multiple members of her family were found to have intestinal polyps, and a sister had been diagnosed with breast cancer at early age. An intronic mutation-T>G transition at the +32 position of intron 8 (c.1026+32 T>G)-was found in this family, with in silico analysis revealing the creation of a new donor splice site. This study confirmed the involvement of PTEN in CS and the variable clinical expressivity of disease
Subject: Gene PTEN
Country: Países Baixos
Editor: Elsevier
Rights: Fechado
Identifier DOI: 10.1016/j.oooo.2018.08.016
Address: https://www.sciencedirect.com/science/article/pii/S221244031831160X
Date Issue: 2019
Appears in Collections:FOP - Artigos e Outros Documentos

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