POLR1C Gene Treacher Collins syndrome type 3 Genetic Test
At DNA Labs UAE, we offer the POLR1C Gene Treacher Collins syndrome type 3 Genetic Test. This test helps diagnose and identify mutations or variants in the POLR1C gene that may be responsible for Treacher Collins syndrome type 3.
Test Components
- Test Name: POLR1C Gene Treacher Collins syndrome type 3 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: Dysmorphology
- Doctor: Pediatrics
- Test Department: Genetics
Pre Test Information
Before undergoing the POLR1C Gene Treacher Collins syndrome type 3 NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by Treacher Collins syndrome type 3.
Test Details
The POLR1C gene is associated with Treacher Collins syndrome type 3, a rare genetic disorder that affects the development of facial bones and tissues. NGS genetic testing, using Next-Generation Sequencing technology, can analyze multiple genes simultaneously, providing a comprehensive assessment of an individual’s genetic makeup.
NGS genetic testing specifically for Treacher Collins syndrome type 3 can identify mutations or variants in the POLR1C gene that may be linked to the disorder. By comparing an individual’s DNA to a reference genome, variations or mutations in the POLR1C gene can be detected, confirming a diagnosis and providing information about the specific genetic cause of the condition.
It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors. They can provide guidance on the implications of the test results, potential treatment options, and counseling for affected individuals and their families.
| Test Name | POLR1C Gene Treacher Collins syndrome type 3 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 | Dysmorphology |
| Doctor | Pediatrics |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for POLR1C Gene Treacher Collins syndrome type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with POLR1C Gene Treacher Collins syndrome type 3 NGS Genetic DNA Test gene POLR1C |
| Test Details |
The POLR1C gene is associated with Treacher Collins syndrome type 3. Treacher Collins syndrome is a rare genetic disorder that affects the development of facial bones and tissues. Type 3 is one of the subtypes of Treacher Collins syndrome, characterized by severe craniofacial abnormalities. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously, providing a comprehensive assessment of an individual’s genetic makeup. In the case of Treacher Collins syndrome type 3, NGS genetic testing can identify mutations or variants in the POLR1C gene that may be responsible for the disorder. NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome. This helps identify any variations or mutations in the POLR1C gene that may be linked to Treacher Collins syndrome type 3. By detecting these genetic changes, NGS testing can assist in confirming a diagnosis and providing information about the specific genetic cause of the condition. It’s important to note that genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors. They can provide guidance on the implications of the test results, potential treatment options, and counseling for affected individuals and their families. |
