Cargando…
Muir-Torre Syndrome: The Importance of a Detailed Family History
Muir-Torre syndrome, a variant of Lynch syndrome or hereditary nonpolyposis colorectal cancer, is an autosomal dominant disease characterized by skin neoplasms (sebaceous or keratoacanthomas) and visceral malignancies. Due to the rarity of the syndrome there are no firm guidelines on how and when to...
Autores principales: | Burris, Christopher K.H., Rodriguez, Maria E., Raven, Meisha L., Reddy, Devasis N., Xu, Yaohui G., Wiggs, Janey L., Potter, Heather D., Albert, Daniel M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6760355/ https://www.ncbi.nlm.nih.gov/pubmed/31692600 http://dx.doi.org/10.1159/000500662 |
Ejemplares similares
-
The role of immunohistochemistry in the Muir-Torre Syndrome
por: Oliveira, Cláudia Marina Puga Barbosa, et al.
Publicado: (2015) -
A Case of Muir-Torre Syndrome
por: Sheth, Radhika, et al.
Publicado: (2021) -
Generational Expression of Muir-Torre Syndrome in a Canadian Family
por: Vanderbeck, Kaitlin Alexandra, et al.
Publicado: (2016) -
Muir Torre syndrome and in vitro fertilization: One family's experience
por: Cox, Surget, et al.
Publicado: (2020) -
Muir Torre syndrome and MSH2 mutations: the importance of dermatological awareness
por: Tischkowitz, M, et al.
Publicado: (2006)