Among hereditary colorectal cancer predisposing syndromes, Lynch syndrome (LS) caused by mutations in DNA mismatch repair genes MLH1, MSH2, MSH6 or PMS2 is the most common. Patients with LS have an increased risk of early onset colon and endometrial cancer, but also other tumors that generally have an earlier onset compared to the general population. However, age at first primary cancer varies within families and genetic anticipation, i.e. decreasing age at onset in successive generations, has been suggested in LS. Anticipation is a well-known phenomenon in e.g neurodegenerative diseases and several reports have studied anticipation in heritable cancer. The purpose of this study is to determine whether anticipation can be shown in a large c...
Background: Existing clinical practice guidelines for carriers of pathogenic variants of DNA mismatc...
BACKGROUND: Existing clinical practice guidelines for carriers of pathogenic variants of DNA mismatc...
PurposeThe clinical consequences of PMS2 germline mutations are poorly understood compared with othe...
Among hereditary colorectal cancer predisposing syndromes, Lynch syndrome (LS) caused by mutations i...
Among hereditary colorectal cancer predisposing syndromes, Lynch syndrome (LS) caused by mutations i...
Lynch syndrome is the commonest inherited cause of colorectal cancer (CRC). Genetic anticipation occ...
PURPOSE: Anticipation (ie, an earlier age at onset in successive generations) is linked to repeat ex...
Background: PMS2-associated Lynch syndrome is characterized by a relatively low colorectal cancer pe...
Lynch syndrome (LS) is the most common form of inherited predisposition to develop cancer mainly in ...
Colorectal cancer is the second most common cancer in women and the third most common cancer in men...
Optimal prevention of hereditary cancer is central and requires initiation of surveillance programme...
Genetic anticipation is the phenomenon in which age of onset of an inherited disorder decreases in s...
Abstract Background Lynch Syndrome is an autosomal dominant cancer syndrome caused by pathogenic ger...
Background: Approximately 10% of Lynch syndrome families have a mutation in MSH6 and fewer families ...
Background Existing clinical practice guidelines for carriers of pathogenic variants of DNA mismatch...
Background: Existing clinical practice guidelines for carriers of pathogenic variants of DNA mismatc...
BACKGROUND: Existing clinical practice guidelines for carriers of pathogenic variants of DNA mismatc...
PurposeThe clinical consequences of PMS2 germline mutations are poorly understood compared with othe...
Among hereditary colorectal cancer predisposing syndromes, Lynch syndrome (LS) caused by mutations i...
Among hereditary colorectal cancer predisposing syndromes, Lynch syndrome (LS) caused by mutations i...
Lynch syndrome is the commonest inherited cause of colorectal cancer (CRC). Genetic anticipation occ...
PURPOSE: Anticipation (ie, an earlier age at onset in successive generations) is linked to repeat ex...
Background: PMS2-associated Lynch syndrome is characterized by a relatively low colorectal cancer pe...
Lynch syndrome (LS) is the most common form of inherited predisposition to develop cancer mainly in ...
Colorectal cancer is the second most common cancer in women and the third most common cancer in men...
Optimal prevention of hereditary cancer is central and requires initiation of surveillance programme...
Genetic anticipation is the phenomenon in which age of onset of an inherited disorder decreases in s...
Abstract Background Lynch Syndrome is an autosomal dominant cancer syndrome caused by pathogenic ger...
Background: Approximately 10% of Lynch syndrome families have a mutation in MSH6 and fewer families ...
Background Existing clinical practice guidelines for carriers of pathogenic variants of DNA mismatch...
Background: Existing clinical practice guidelines for carriers of pathogenic variants of DNA mismatc...
BACKGROUND: Existing clinical practice guidelines for carriers of pathogenic variants of DNA mismatc...
PurposeThe clinical consequences of PMS2 germline mutations are poorly understood compared with othe...