PIK3CA Gene Cowden syndrome type 5 Genetic Test
Welcome to DNA Labs UAE, a leading genetic lab offering the PIK3CA Gene Cowden syndrome type 5 Genetic Test. This blog post will provide you with detailed information about the test, including its components, price, sample condition, report delivery time, method, test type, and more.
Test Details
The PIK3CA gene is a gene that provides instructions for making a protein called phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha isoform. This protein is involved in cell signaling pathways that regulate cell growth, division, and survival.
Cowden syndrome is a rare genetic disorder characterized by multiple noncancerous, tumor-like growths called hamartomas. It is caused by mutations in the PTEN gene, which is involved in regulating cell division and preventing cells from growing and dividing too rapidly or uncontrollably. However, there is a subtype of Cowden syndrome called Cowden syndrome type 5, which is associated with mutations in the PIK3CA gene instead of the PTEN gene. Cowden syndrome type 5 is characterized by the development of hamartomas and an increased risk of certain types of cancer, such as breast, thyroid, and endometrial cancer.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously to identify mutations or variations that may be associated with a specific condition or disease. In the case of Cowden syndrome type 5, an NGS genetic test can be used to analyze the PIK3CA gene for mutations or variations that may be causative or associated with the syndrome. This type of genetic testing can help with the diagnosis of Cowden syndrome type 5 and may also provide information about the individual’s risk of developing certain types of cancer. It can also be useful for identifying family members who may be at risk of inheriting the mutation and developing the syndrome.
It is important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and interpretation of the results.
Test Components
- Test Name: PIK3CA Gene Cowden syndrome 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
Prior to undergoing the PIK3CA Gene Cowden syndrome type 5 NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with the PIK3CA Gene Cowden syndrome type 5 NGS Genetic DNA Test gene PIK3CA.
Thank you for choosing DNA Labs UAE for your genetic testing needs. If you have any further questions or would like to schedule an appointment, please contact our team.
| Test Name | PIK3CA Gene Cowden syndrome 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 PIK3CA Gene Cowden syndrome type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PIK3CA Gene Cowden syndrome type 5 NGS Genetic DNA Test gene PIK3CA |
| Test Details |
The PIK3CA gene is a gene that provides instructions for making a protein called phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha isoform. This protein is involved in cell signaling pathways that regulate cell growth, division, and survival. Cowden syndrome is a rare genetic disorder characterized by multiple noncancerous, tumor-like growths called hamartomas. It is caused by mutations in the PTEN gene, which is involved in regulating cell division and preventing cells from growing and dividing too rapidly or uncontrollably. However, there is a subtype of Cowden syndrome called Cowden syndrome type 5, which is associated with mutations in the PIK3CA gene instead of the PTEN gene. Cowden syndrome type 5 is characterized by the development of hamartomas and an increased risk of certain types of cancer, such as breast, thyroid, and endometrial cancer. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously to identify mutations or variations that may be associated with a specific condition or disease. In the case of Cowden syndrome type 5, an NGS genetic test can be used to analyze the PIK3CA gene for mutations or variations that may be causative or associated with the syndrome. This type of genetic testing can help with the diagnosis of Cowden syndrome type 5 and may also provide information about the individual’s risk of developing certain types of cancer. It can also be useful for identifying family members who may be at risk of inheriting the mutation and developing the syndrome. It is important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and interpretation of the results. |
