A Novel Mutation of MSH2 Gene in a Patient with Lynch Syndrome Presenting with Thirteen Metachronous Malignancies

Lynch syndrome (LS), also known as hereditary nonpolyposis colorectal cancer (HNPCC), accounts for 2–3% of all colorectal cancers. This autosomal dominant disorder is associated with a predisposition to endometrial, stomach, small bowel, pancreatic, biliary tract, ovary, urinary tract, brain, and sk...

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Detalles Bibliográficos
Autores principales: Silinskaite, Ugne, Gavelienė, Edita, Stulpinas, Rokas, Janavicius, Ramunas, Poskus, Tomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10488139/
https://www.ncbi.nlm.nih.gov/pubmed/37685569
http://dx.doi.org/10.3390/jcm12175502

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10488139/
https://www.ncbi.nlm.nih.gov/pubmed/37685569
http://dx.doi.org/10.3390/jcm12175502

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