Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/339417
Type: Artigo
Title: Exuberant manifestation of neurofibromatosis type 1 affeting 3 generation: delayed diagnosis and the importance of the mtulidisciplinary approach
Author: Tolentino, Elen de Souza
de Souza Pinto, Gustavo Nascimento
Maciel, Larissa
Soares, Cleverson Teixeira
Lara, Vanessa Soares
Casaroto Moreschi, Ana Regina
Abstract: Neurofibromatosis type 1 (NF1) is an autosomal dominant inherited disorder caused by mutations of chromosome 17. The NF1 clinical diagnosis is based on pre-established criteria, including the presence of cutaneous neurofibromas, cafe au lait spots, and iris (Lisch) nodules. Early detection and a multidisciplinary approach are essential for the prevention of complications, including problems of function, aesthetics, and self-esteem, as well as the occurrence of malignant transformation. This study reports a case of an exuberant NF1 manifestation diagnosed by a dental surgeon, whose investigation of a family led to the diagnosis of NF1, with different expressivities, in 3 generations
Subject: Neurofibromatose 1
Country: Países Baixos
Editor: Elsevier
Rights: Fechado
Identifier DOI: 10.1016/j.oooo.2019.03.003
Address: https://www.sciencedirect.com/science/article/pii/S2212440319303931
Date Issue: 2019
Appears in Collections:FOP - Artigos e Outros Documentos

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