NDUFA13 Gene Hurthle Cell Thyroid Carcinoma Genetic Test
Welcome to DNA Labs UAE, where we provide comprehensive genetic testing services. In this blog post, we will discuss the NDUFA13 gene, germline NDUFA13 mutation, and the NGS genetic test for Hurthle cell thyroid carcinoma.
Test Name: NDUFA13 Gene Hurthle Cell Thyroid Carcinoma due to Germline NDUFA13 Mutation Genetic Test
- Components: NGS Technology
- Price: 4400.0 AED
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Test Type: Cancer
- Doctor: Oncologist
- Test Department: Genetics
Pre Test Information
If you are considering the NDUFA13 Gene Hurthle Cell Thyroid Carcinoma Genetic Test, it is important to provide your clinical history to the oncologist. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by NDUFA13 Gene Hurthle Cell Thyroid Carcinoma due to germline NDUFA13 mutation.
Test Details
The NDUFA13 gene is responsible for producing a protein called NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 13. This protein is part of the mitochondrial complex I, which plays a role in the electron transport chain and energy production within cells.
Hurthle cell thyroid carcinoma is a type of thyroid cancer that originates from the follicular cells of the thyroid gland. It is characterized by the presence of Hurthle cells, which are large cells with abundant eosinophilic cytoplasm.
A germline NDUFA13 mutation refers to a genetic mutation in the NDUFA13 gene that is present in the germline cells. These cells give rise to eggs or sperm, meaning the mutation can be inherited from one or both parents and passed on to future generations.
NGS (Next-Generation Sequencing) Genetic Test is a technique used to analyze multiple genes simultaneously and identify genetic mutations or variations associated with diseases or conditions. In the context of NDUFA13 gene and Hurthle cell thyroid carcinoma, an NGS genetic test can identify mutations in the NDUFA13 gene associated with this specific type of thyroid cancer.
By identifying a germline NDUFA13 mutation through NGS genetic testing, individuals at risk for Hurthle cell thyroid carcinoma can be identified early on. This allows for more effective screening, surveillance, and management strategies to reduce the risk or detect the cancer at an earlier stage. Additionally, it aids in genetic counseling for affected individuals and their families.
Conclusion
The NDUFA13 Gene Hurthle Cell Thyroid Carcinoma Genetic Test offered by DNA Labs UAE provides valuable insights into the risk of developing Hurthle cell thyroid carcinoma. Early identification of germline NDUFA13 mutations allows for proactive measures to manage and reduce the risk of this specific type of thyroid cancer. Consult with our oncologist and genetic counselors to understand the implications of NDUFA13 gene mutations and take control of your health.
Test Name | NDUFA13 Gene Hurthle cell thyroid carcinoma due to germline NDUFA13 mutation 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 NDUFA13 Gene Hurthle cell thyroid carcinoma, due to germline NDUFA13 mutation NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFA13 Gene Hurthle cell thyroid carcinoma, due to germline NDUFA13 mutation NGS Genetic DNA Test gene NDUFA13 |
Test Details |
The NDUFA13 gene is responsible for providing instructions to produce a protein called NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 13. This protein is a part of the mitochondrial complex I, which is involved in the electron transport chain and energy production within cells. Hurthle cell thyroid carcinoma is a type of thyroid cancer that originates from the follicular cells of the thyroid gland. It is characterized by the presence of Hurthle cells, which are large cells with abundant eosinophilic cytoplasm. A germline NDUFA13 mutation refers to a genetic mutation in the NDUFA13 gene that is present in the germline cells, which are the cells that give rise to eggs or sperm. This means that the mutation can be inherited from one or both parents and can be passed on to future generations. NGS (Next-Generation Sequencing) Genetic Test is a technique used to analyze multiple genes simultaneously and identify genetic mutations or variations that may be associated with certain diseases or conditions. In the context of NDUFA13 gene and Hurthle cell thyroid carcinoma, an NGS genetic test can be used to identify mutations in the NDUFA13 gene that may be associated with the development of this specific type of thyroid cancer. By identifying a germline NDUFA13 mutation through NGS genetic testing, individuals at risk for Hurthle cell thyroid carcinoma can be identified early on. This can lead to more effective screening, surveillance, and management strategies to reduce the risk or detect the cancer at an earlier stage. Additionally, it can help in genetic counseling for affected individuals and their families. |