Cargando…
Early-onset breast cancer in a Lebanese family with Lynch syndrome due to MSH2 gene mutation
BACKGROUND: There are still controversies about the integration of breast cancer as a part of the disease spectrum in Lynch syndrome. METHODS: A regular follow-up of a Lebanese pedigree with Lynch syndrome due to a point mutation of MSH2 gene at the splice donor site of intron 3 started in 1996. RES...
Autores principales: | Akoum, Riad, Ghaoui, Albert, Brihi, Emile, Ghabash, Maroun, Hajjar, Nicolas |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2692982/ https://www.ncbi.nlm.nih.gov/pubmed/19476642 http://dx.doi.org/10.1186/1897-4287-7-10 |
Ejemplares similares
-
An unusual tumor spectrum in Lynch syndrome caused by MSH6 mutation
por: Perrier, Renee L, et al.
Publicado: (2010) -
Frequency and Variability of Genomic Rearrangements on MSH2 in Spanish Lynch Syndrome Families
por: Romero, Atocha, et al.
Publicado: (2013) -
A Hereditable Mutation of MSH2 Gene Associated with Lynch Syndrome in a Five Generation Chinese Family
por: Shao, Wei-Hua, et al.
Publicado: (2020) -
UMD-MLH1/MSH2/MSH6 databases: description and analysis of genetic variations in French Lynch syndrome families
por: Grandval, Philippe, et al.
Publicado: (2013) -
Novel germline MSH2 mutation in lynch syndrome patient surviving multiple cancers
por: Janavicius, Ramunas, et al.
Publicado: (2012)