リンチ症候群は通常、MLH1、MSH2、MSH6、PMS2 などのミスマッチ修復遺伝子の変異によって特徴づけられます。これらの遺伝子は、細胞分裂中に起こる DNA 損傷を修復する役割を担っています。 リンチ症候群は、主に大腸癌および子宮内膜癌のリスク増加と関連しています。リンチ症候群の患者で ACC が発症するケースは比較的少ないです。
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