PMS1 Gene Nonpolyposis Hereditary Colon Cancer
Welcome to DNA Labs UAE, a leading genetic lab specializing in DNA testing. In this blog post, we will discuss the PMS1 gene nonpolyposis hereditary colon cancer and the PMS1 related genetic test offered at our lab.
Test Details
The PMS1 gene, also known as Postmeiotic Segregation Increased 1, is a gene involved in DNA mismatch repair (MMR). Mutations in the PMS1 gene can lead to a condition called PMS1-related nonpolyposis hereditary colon cancer, also known as Lynch syndrome or hereditary nonpolyposis colorectal cancer.
Lynch syndrome is an inherited condition that increases the risk of developing various types of cancer, particularly colorectal cancer. Individuals with Lynch syndrome have a higher chance of developing colon, endometrial, ovarian, stomach, urinary tract, and other cancers.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. In the context of PMS1-related Lynch syndrome, NGS genetic testing can identify mutations or variations in the PMS1 gene, as well as other genes associated with Lynch syndrome.
The NGS genetic test for PMS1-related Lynch syndrome involves obtaining a DNA sample, usually through a blood sample or saliva collection. The DNA is then sequenced using advanced sequencing technology to identify any genetic variations or mutations in the PMS1 gene and other relevant genes.
This test can help determine an individual’s risk of developing Lynch syndrome-associated cancers and guide appropriate medical management and surveillance.
It is important to note that genetic testing for PMS1-related Lynch syndrome should be performed by a qualified genetic counselor or healthcare professional. They can provide appropriate pre-test counseling, interpret the results, and provide guidance on potential preventive measures or surveillance strategies based on the test results.
Test Name: PMS1 Gene Nonpolyposis Hereditary Colon Cancer PMS1 Related Genetic Test
Components: PMS1 gene analysis
Price: 4400.0 AED
Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery: 3 to 4 Weeks
Method: NGS Technology
Test Type: Cancer
Doctor: Oncologist
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for PMS1 Gene Nonpolyposis Hereditary Colon Cancer, PMS1 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PMS1 Gene Nonpolyposis Hereditary Colon Cancer, PMS1 related NGS Genetic DNA Test gene PMS1.
Thank you for reading our blog post on PMS1 gene nonpolyposis hereditary colon cancer and the PMS1 related genetic test. If you have any further questions or would like to schedule an appointment, please contact DNA Labs UAE.
| Test Name | PMS1 Gene Nonpolyposis hereditary colon cancer PMS1 related Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Cancer |
| Doctor | Oncologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for PMS1 Gene Nonpolyposis hereditary colon cancer, PMS1 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PMS1 Gene Nonpolyposis hereditary colon cancer, PMS1 related NGS Genetic DNA Test gene PMS1 |
| Test Details |
PMS1 gene, also known as Postmeiotic Segregation Increased 1, is a gene involved in DNA mismatch repair (MMR). Mutations in the PMS1 gene can lead to a condition called PMS1-related nonpolyposis hereditary colon cancer (also known as Lynch syndrome or hereditary nonpolyposis colorectal cancer). Lynch syndrome is an inherited condition that increases the risk of developing various types of cancer, particularly colorectal cancer. Individuals with Lynch syndrome have a higher chance of developing colon, endometrial, ovarian, stomach, urinary tract, and other cancers. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. In the context of PMS1-related Lynch syndrome, NGS genetic testing can identify mutations or variations in the PMS1 gene, as well as other genes associated with Lynch syndrome. The NGS genetic test for PMS1-related Lynch syndrome involves obtaining a DNA sample, usually through a blood sample or saliva collection. The DNA is then sequenced using advanced sequencing technology to identify any genetic variations or mutations in the PMS1 gene and other relevant genes. This test can help determine an individual’s risk of developing Lynch syndrome-associated cancers and guide appropriate medical management and surveillance. It is important to note that genetic testing for PMS1-related Lynch syndrome should be performed by a qualified genetic counselor or healthcare professional. They can provide appropriate pre-test counseling, interpret the results, and provide guidance on potential preventive measures or surveillance strategies based on the test results. |
