Pediatric manifestations of Lynch Syndrome: A single center experience

Lynch syndrome is an autosomal dominant condition caused by a heterozygous variation in one of the DNA mismatch repair (MMR) genes that pre-disposes individuals to early onset colorectal cancers and other malignancies. Lynch syndrome is generally considered an adult-onset disorder, with malignancy r...

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Detalles Bibliográficos
Autores principales: MacArthur, Taleen A., Ongie, Laura J., Lanpher, Brendan C., Ishitani, Michael B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9609293/
https://www.ncbi.nlm.nih.gov/pubmed/36313796
http://dx.doi.org/10.1016/j.epsc.2022.102431

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9609293/
https://www.ncbi.nlm.nih.gov/pubmed/36313796
http://dx.doi.org/10.1016/j.epsc.2022.102431

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