Mismatch repair cancer syndrome 4

MONDO:0030843

An autosomal recessive constitutional mismatch repair deficiency syndrome caused by pathogenic variants in the PMS2 mismatch repair gene. It is characterized by a high risk of childhood cancers, including hematological malignancies and brain tumors, as well as colorectal cancers with polyposis.

Also known as: MMRCS4, PMS2-related constitutional mismatch repair deficiency syndrome, mismatch repair cancer syndrome 4

26 clinical trials for this condition and its sub-types.

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