Ontology highlight
ABSTRACT:
SUBMITTER: Rittberg R
PROVIDER: S-EPMC7985791 | biostudies-literature | 2021 Feb
REPOSITORIES: biostudies-literature
Rittberg Rebekah R Harlos Craig C Rothenmund Heidi H Das Anirban A Tabori Uri U Sinha Namita N Singh Harminder H Chodirker Bernie B Kim Christina A CA
Current oncology (Toronto, Ont.) 20210201 1
Constitutional mismatch repair deficiency (CMMRD) is a rare autosomal recessive hereditary cancer syndrome due to biallelic germline mutation involving one of the four DNA mismatch repair genes. Here we present a case of a young female with CMMRD, homozygous for the c.2002A>G mutation in the <i>PMS2</i> gene. She developed an early stage adenocarcinoma of the colon at the age of 14. Surveillance MRI of the brain at age 18 resulted in the detection of an asymptomatic brain cancer. On resection, t ...[more]