TY - JOUR
T1 - A Novel Case of Biallelic MLH3 Variants in a Patient With Rectal Cancer and Polyps
AU - Johannesen, Katrine M.
AU - Karstensen, John Gásdal
AU - Rasmussen, Andreas Ørslev
AU - Scott, Emma Adine Hoxer
AU - Birkedal, Ulf
AU - Hansen, Thomas v. O.
AU - Steenholdt, Casper
AU - Jelsig, Anne Marie
N1 - © 2025 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
PY - 2025
Y1 - 2025
N2 - An increasing number of autosomal recessive forms of adenomatous polyposis have been described, but some in very few cases. Here, we describe a rare case of biallelic germline pathogenic variants in the MLH3 gene, implicating it as a potential cause of early colorectal cancer. The patient, a 47-year-old woman, presented with rectal bleeding, leading to the discovery of a malignant rectal tumor and adenomas during colonoscopy. Histopathological examination confirmed adenocarcinoma without microsatellite instability, and genetic testing identified two likely pathogenic frameshift variants in MLH3 located in trans. These findings contribute to the expanding knowledge of MLH3-related polyposis and colorectal cancer and underscore the need for further research into the gene's broader implications, including its potential role in cancer and infertility pathways.
AB - An increasing number of autosomal recessive forms of adenomatous polyposis have been described, but some in very few cases. Here, we describe a rare case of biallelic germline pathogenic variants in the MLH3 gene, implicating it as a potential cause of early colorectal cancer. The patient, a 47-year-old woman, presented with rectal bleeding, leading to the discovery of a malignant rectal tumor and adenomas during colonoscopy. Histopathological examination confirmed adenocarcinoma without microsatellite instability, and genetic testing identified two likely pathogenic frameshift variants in MLH3 located in trans. These findings contribute to the expanding knowledge of MLH3-related polyposis and colorectal cancer and underscore the need for further research into the gene's broader implications, including its potential role in cancer and infertility pathways.
U2 - 10.1111/cge.14689
DO - 10.1111/cge.14689
M3 - Letter
C2 - 39789695
SN - 0009-9163
VL - 107
SP - 480
EP - 482
JO - Clinical Genetics
JF - Clinical Genetics
IS - 4
ER -