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MSH6 Gene Colorectal Cancer Hereditary Nonpolyposis Type 5 Genetic Test Cost

Name: MSH6 Gene Colorectal Cancer Hereditary Nonpolyposis Type 5 Genetic Test Cost
SKU: TEST-4471
Price: 4400 AED
Availability: InStock

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The MSH6 gene plays a crucial role in DNA mismatch repair, a process essential for maintaining genomic stability. Mutations in the MSH6 gene are associated with Lynch syndrome, also known as Hereditary Nonpolyposis Colorectal Cancer (HNPCC) Type 5, which significantly increases the risk of developing colorectal cancer and other types of cancer. The MSH6 Gene Colorectal Cancer Hereditary Nonpolyposis Type 5 Genetic Test is a specialized diagnostic tool designed to detect mutations in the MSH6 gene. This test is pivotal for individuals with a family history of Lynch syndrome or those who meet certain clinical criteria, as it can confirm the diagnosis and inform appropriate cancer surveillance and management strategies. The test is available at DNA Labs UAE, a leading facility in genetic diagnostics, at a cost of 4400 AED. Identifying MSH6 gene mutations not only aids in the early detection and prevention of colorectal cancer in at-risk individuals but also facilitates informed decisions regarding family planning.

Description

MSH6 Gene Colorectal Cancer Hereditary Nonpolyposis Type 5 Genetic Test

Components: MSH6 Gene Colorectal cancer hereditary nonpolyposis type 5 Genetic Test

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 MSH6 Gene Colorectal cancer, hereditary nonpolyposis type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MSH6 Gene Colorectal cancer, hereditary nonpolyposis type 5 NGS Genetic DNA Test gene MSH6

Test Details:

The MSH6 gene is one of the DNA mismatch repair genes involved in repairing errors that occur during DNA replication. Mutations in the MSH6 gene can lead to a condition called hereditary nonpolyposis colorectal cancer (HNPCC), also known as Lynch syndrome.

HNPCC is an inherited condition that increases the risk of developing colorectal cancer, as well as other types of cancer such as endometrial, ovarian, and stomach cancer. Individuals with HNPCC have a 50-80% lifetime risk of developing colorectal cancer.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously for mutations. In the case of HNPCC, NGS testing can be used to identify mutations in the MSH6 gene and other genes associated with the condition.

NGS genetic testing for HNPCC can help identify individuals who have a higher risk of developing colorectal cancer and other associated cancers. This information can be used to guide personalized screening and surveillance strategies, as well as to inform family members about their own risk of developing cancer.

It is important to note that genetic testing for HNPCC should be done under the guidance of a healthcare professional, such as a genetic counselor or a medical geneticist, who can help interpret the results and provide appropriate recommendations based on an individual’s personal and family history.

Test Name	MSH6 Gene Colorectal cancer hereditary nonpolyposis type 5 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 MSH6 Gene Colorectal cancer, hereditary nonpolyposis type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MSH6 Gene Colorectal cancer, hereditary nonpolyposis type 5 NGS Genetic DNA Test gene MSH6
Test Details	The MSH6 gene is one of the DNA mismatch repair genes involved in repairing errors that occur during DNA replication. Mutations in the MSH6 gene can lead to a condition called hereditary nonpolyposis colorectal cancer (HNPCC), also known as Lynch syndrome. HNPCC is an inherited condition that increases the risk of developing colorectal cancer, as well as other types of cancer such as endometrial, ovarian, and stomach cancer. Individuals with HNPCC have a 50-80% lifetime risk of developing colorectal cancer. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously for mutations. In the case of HNPCC, NGS testing can be used to identify mutations in the MSH6 gene and other genes associated with the condition. NGS genetic testing for HNPCC can help identify individuals who have a higher risk of developing colorectal cancer and other associated cancers. This information can be used to guide personalized screening and surveillance strategies, as well as to inform family members about their own risk of developing cancer. It is important to note that genetic testing for HNPCC should be done under the guidance of a healthcare professional, such as a genetic counselor or a medical geneticist, who can help interpret the results and provide appropriate recommendations based on an individual’s personal and family history.