Mismatch repair cancer syndrome 3

An autosomal recessive constitutional mismatch repair deficiency syndrome caused by pathogenic variants in the MSH6 mismatch repair gene is characterized by a high risk of childhood cancers, including hematological malignancies, brain tumors, and colorectal

Also known as: MMRCS3, MSH6-related constitutional mismatch repair deficiency syndrome, mismatch repair cancer syndrome 3

3 clinical trials for this condition and its sub-types, 0 tagged with Mismatch repair cancer syndrome 3 itself.