The purpose of this study is to find out the proportion of patients diagnosed with Lynch syndrome in colorectal cacner patients meeting Chinese Lynch syndrome criteria. Besides, this study is aimed to analyze the clinical characteristics and germline mutation of Lynch syndrome in Chinese population.
1. Detect germline mutation (by next-generation squencing) in probands. 2. Verify the germline mutation in blood relatives whose proband has known germline mutation(s). 3. Analyze the test data with clinical and family information. Diagnose Lynch syndrome in the included population. 4. Analyze the clinical characteristics and germline mutation of Lynch syndrome in Chinese population.
Study Type
OBSERVATIONAL
Enrollment
100
Use next-generation sequencing to test germline mutation.
Jiangsu Province Hospital
Nanjing, Jiangsu, China
West China Hospital
Chengdu, Sichuan, China
The second affiliated hospital of Zhejiang University
Hangzhou, Zhejinag, China
Pathogenic germline mutation
Pathogenic germline mutation using next-generation sequencing with a targeted panel.
Time frame: Upon completion of study, on average 2 years.
Variant of uncertain significance of germline mutation
Variant of uncertain significance using next-generation sequencing with a targeted panel.
Time frame: Upon completion of study, on average 2 years.
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