BMPR1A Gene Polyposis Syndrome Hereditary Mixed Type 2 Genetic Test
Components: BMPR1A Gene Polyposis syndrome, hereditary mixed type 2 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 BMPR1A Gene Polyposis syndrome, hereditary mixed type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BMPR1A Gene Polyposis syndrome, hereditary mixed type 2 NGS Genetic DNA Test gene BMPR1A
Test Details: BMPR1A Gene Polyposis syndrome, hereditary mixed type 2 is a genetic disorder characterized by the development of multiple polyps in the colon and rectum. It is caused by mutations in the BMPR1A gene, which is involved in the regulation of cell growth and division. NGS Genetic Test refers to Next-Generation Sequencing Genetic Test, which is a high-throughput sequencing technology used to analyze multiple genes simultaneously. In the context of BMPR1A Gene Polyposis syndrome, hereditary mixed type 2, NGS Genetic Test can be used to identify mutations in the BMPR1A gene that are associated with the disorder. The NGS Genetic Test involves sequencing the DNA of an individual to identify any genetic variations or mutations in the BMPR1A gene. This can help in confirming a diagnosis of BMPR1A Gene Polyposis syndrome and provide information about the specific mutation present in the individual. Genetic testing for BMPR1A Gene Polyposis syndrome, hereditary mixed type 2 can be useful for individuals with a family history of the disorder or those who exhibit symptoms of the condition. It can help in early detection, risk assessment, and management of the disorder. Additionally, genetic testing can also be used for carrier screening and prenatal diagnosis in families with a known BMPR1A gene mutation. It is important to note that genetic testing should be done under the guidance of a healthcare professional or a genetic counselor who can provide appropriate counseling and interpretation of the results.
Test Name | BMPR1A Gene Polyposis syndrome hereditary mixed type 2 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 BMPR1A Gene Polyposis syndrome, hereditary mixed type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BMPR1A Gene Polyposis syndrome, hereditary mixed type 2 NGS Genetic DNA Test gene BMPR1A |
Test Details |
BMPR1A Gene Polyposis syndrome, hereditary mixed type 2 is a genetic disorder characterized by the development of multiple polyps in the colon and rectum. It is caused by mutations in the BMPR1A gene, which is involved in the regulation of cell growth and division. NGS Genetic Test refers to Next-Generation Sequencing Genetic Test, which is a high-throughput sequencing technology used to analyze multiple genes simultaneously. In the context of BMPR1A Gene Polyposis syndrome, hereditary mixed type 2, NGS Genetic Test can be used to identify mutations in the BMPR1A gene that are associated with the disorder. The NGS Genetic Test involves sequencing the DNA of an individual to identify any genetic variations or mutations in the BMPR1A gene. This can help in confirming a diagnosis of BMPR1A Gene Polyposis syndrome and provide information about the specific mutation present in the individual. Genetic testing for BMPR1A Gene Polyposis syndrome, hereditary mixed type 2 can be useful for individuals with a family history of the disorder or those who exhibit symptoms of the condition. It can help in early detection, risk assessment, and management of the disorder. Additionally, genetic testing can also be used for carrier screening and prenatal diagnosis in families with a known BMPR1A gene mutation. It is important to note that genetic testing should be done under the guidance of a healthcare professional or a genetic counselor who can provide appropriate counseling and interpretation of the results. |