遗传性肿瘤综合症-ag亚洲国际厅

overview

cancer is a common disease, experts find that about 10% of most cancer types are due to inherited gene changes. everyone has two copies of each gene, one from each parent. most people are born with two normal copies of each gene. hereditary cancers occur when a person is born with changes or mutations in one copy of a damage-controlling gene which normally protects against cancer. in the majority of these cases, the changes were inherited from the mother or father. the medical community uses the term "genetic susceptibility" to describe the high risk for cancer in people with an inherited mutation.

utumorrisk can simultaneously test 43 kinds of tumor-related genetic mutation, including all of the exons of 211 gene.

cancer list

application

  • help the people who had a family history of cancer to understand their cancer risk;
  • improves understanding about cancer risk to guide medical decisions about the best way to manage their risk;
  • helps you and your family understand and manage the risk of cancer.

advantage

advanced:the illumina high-throughput sequencing system and bioinformatics analysis platform are adopted.

comprehensive:our testing include 60 pharmacogenomics related genes, comprehensive help doctors and patients choose the right drugs.

quick: we will provide genetic testing report to you within 1-2 weeks.

professional: the interpretation of the test is based upon our powerful database including both the authoritative databases and the latest clinical research results.

检测流程 遗传咨询&知情同意 样本采集 dna变异信息检测 遗传信息解读 健康生活指导

faq:

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