PMS2 germline mutation c.1577delA (p.Asp526Alafs(∗)69)-induced Lynch syndrome-associated endometrial cancer: A case report

RATIONALE: Lynch syndrome (LS) is an autosomal dominant cancer predisposition condition caused by germline heterozygous mutations in mismatch repair (MMR) genes. However, as one of the MMR genes, PMS2 mutation-induced LS-associated endometrial cancer (LSAEC) was rarely reported. PATIENT CONCERNS: A...

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Detalles Bibliográficos
Autores principales: Cui, Man-Hua, Zhang, Xi-Wen, Yu, Tong, Huang, Dong-Wei, Jia, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
5600
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6940048/
https://www.ncbi.nlm.nih.gov/pubmed/31860975
http://dx.doi.org/10.1097/MD.0000000000018279

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6940048/
https://www.ncbi.nlm.nih.gov/pubmed/31860975
http://dx.doi.org/10.1097/MD.0000000000018279

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