A Novel Mutation of
detection
hereditary nonpolyposis colorectal cancer
lynch syndrome
metachronous cancer
multiple malignancies
surveillance
tumor
Journal
Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588
Informations de publication
Date de publication:
24 Aug 2023
24 Aug 2023
Historique:
received:
17
07
2023
revised:
21
08
2023
accepted:
22
08
2023
medline:
9
9
2023
pubmed:
9
9
2023
entrez:
9
9
2023
Statut:
epublish
Résumé
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 skin tumors. Lynch syndrome is caused by the mutation of the
Identifiants
pubmed: 37685569
pii: jcm12175502
doi: 10.3390/jcm12175502
pmc: PMC10488139
pii:
doi:
Types de publication
Journal Article
Langues
eng
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