OTC Gene Ornithine transcarbamoylase deficiency Genetic Test
At DNA Labs UAE, we offer the OTC Gene Ornithine transcarbamoylase deficiency Genetic Test to help diagnose and provide valuable information for individuals affected by this rare genetic disorder.
Test Details
The OTC gene (ornithine transcarbamoylase) deficiency is a rare genetic disorder that affects the urea cycle, responsible for removing ammonia from the body. This deficiency is caused by mutations in the OTC gene, responsible for producing the enzyme ornithine transcarbamoylase.
Our NGS (Next-Generation Sequencing) technology allows for a more comprehensive analysis of the genetic cause of the disorder. By analyzing multiple genes simultaneously, we can identify mutations in the OTC gene, aiding in diagnosis, identifying carriers, and providing valuable information for genetic counseling and family planning.
Additionally, NGS genetic testing can assist in the development of targeted treatments and personalized medicine approaches for individuals with OTC gene deficiency.
Test Components
- Test Name: OTC Gene Ornithine transcarbamoylase deficiency 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: Metabolic Disorders
- Doctor: General Physician
- Test Department: Genetics
Pre Test Information
Prior to the OTC Gene Ornithine transcarbamoylase deficiency NGS Genetic DNA Test, it is important to provide the clinical history of the patient. A Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by Ornithine transcarbamoylase deficiency.
Cost and Diagnosis
The cost of the OTC Gene Ornithine transcarbamoylase deficiency Genetic Test is 4400.0 AED. The test can help diagnose individuals with the condition, identify carriers of the mutated gene, and provide valuable information for genetic counseling and family planning.
Conclusion
The OTC Gene Ornithine transcarbamoylase deficiency Genetic Test offered by DNA Labs UAE is a comprehensive and advanced genetic testing option. It allows for the identification of mutations in the OTC gene, aiding in diagnosis, genetic counseling, and personalized treatment approaches. With a focus on Metabolic Disorders and supported by NGS Technology, our test can provide valuable insights for individuals affected by OTC gene deficiency.
| Test Name | OTC Gene Ornithine transcarbamoylase deficiency 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 | Metabolic Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for OTC Gene Ornithine transcarbamoylase deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Ornithine transcarbamoylase deficiency |
| Test Details |
OTC gene (ornithine transcarbamoylase) deficiency is a rare genetic disorder that affects the urea cycle, which is responsible for removing ammonia from the body. This deficiency is caused by mutations in the OTC gene, which is responsible for producing the enzyme ornithine transcarbamoylase. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of OTC gene deficiency, NGS genetic testing can be used to identify mutations in the OTC gene, allowing for a more comprehensive analysis of the genetic cause of the disorder. NGS genetic testing for OTC gene deficiency can help diagnose individuals with the condition, identify carriers of the mutated gene, and provide valuable information for genetic counseling and family planning. It can also aid in the development of targeted treatments and personalized medicine approaches for individuals with OTC gene deficiency. |
