Clinical Updates and Surveillance Recommendations for DNA Replication Repair Deficiency Syndromes in Children and Young Adults

A Das, SP MacFarland, J Meade… - Clinical Cancer …, 2024 - aacrjournals.org
Replication repair deficiency (RRD) is a pan-cancer mechanism characterized by
abnormalities in the DNA mismatch repair (MMR) system due to pathogenic variants in the …

Strong hereditary predispositions to colorectal cancer

S Hryhorowicz, M Kaczmarek-Ryś, E Lis-Tanaś… - Genes, 2022 - mdpi.com
Cancer is one of the most common causes of death worldwide. A strong predisposition to
cancer is generally only observed in colorectal cancer (5% of cases) and breast cancer (2 …

Diagnostic criteria for constitutional mismatch repair deficiency (CMMRD): recommendations from the international consensus working group

M Aronson, C Colas, A Shuen, H Hampel… - Journal of medical …, 2022 - jmg.bmj.com
Background Constitutional mismatch repair deficiency syndrome (CMMRD) is the most
aggressive cancer predisposition syndrome associated with multiorgan cancers, often …

Evaluation of the Potential of Lactobacillus paracasei Adjuncts for Flavor Compounds Development and Diversification in Short-Aged Cheddar Cheese

E Stefanovic, KN Kilcawley, C Roces, MC Rea… - Frontiers in …, 2018 - frontiersin.org
The non-starter microbiota of Cheddar cheese mostly comprises mesophilic lactobacilli,
such as Lactobacillus casei, Lactobacillus paracasei, Lactobacillus rhamnosus, and …

Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy

M Suerink, T Ripperger, L Messiaen… - Journal of medical …, 2019 - jmg.bmj.com
Constitutional mismatch repair deficiency (CMMRD) is a rare childhood cancer
predisposition syndrome caused by biallelic germline mutations in one of four mismatch …

PMS2-associated Lynch syndrome: Past, present and future

KD Andini, M Nielsen, M Suerink… - Frontiers in …, 2023 - frontiersin.org
Carriers of any pathogenic variant in one of the MMR genes (path_MMR carriers) were
traditionally thought to be at comparable risk of developing a range of different …

Café au lait spots: when and how to pursue their genetic origins

L Lalor, OMT Davies, D Basel, DH Siegel - Clinics in dermatology, 2020 - Elsevier
Café au lait spots are common birthmarks seen sporadically and in association with several
genetic syndromes. Dermatologists are often asked to evaluate these birthmarks both by …

Constitutional mismatch repair deficiency is the diagnosis in 0.41% of pathogenic NF1/SPRED1 variant negative children suspected of sporadic neurofibromatosis …

JA Perez-Valencia, R Gallon, Y Chen, J Koch… - Genetics in …, 2020 - nature.com
Purpose Biallelic germline mismatch repair (MMR) gene pathogenic variants (PVs) cause
constitutional MMR deficiency (CMMRD), a highly penetrant childhood cancer syndrome …

The changing landscape of Lynch syndrome due to PMS2 mutations

J Blount, A Prakash - Clinical genetics, 2018 - Wiley Online Library
DNA repair pathways are essential for cellular survival as our DNA is constantly under
assault from both exogenous and endogenous DNA damaging agents. Five major …

Immune Checkpoint Inhibition as Primary Adjuvant Therapy for an IDH1-Mutant Anaplastic Astrocytoma in a Patient with CMMRD: A Case Report—Usage of Immune …

R Rittberg, C Harlos, H Rothenmund, A Das, U Tabori… - Current …, 2021 - mdpi.com
Constitutional mismatch repair deficiency (CMMRD) is a rare autosomal recessive
hereditary cancer syndrome due to biallelic germline mutation involving one of the four DNA …