ZIC1 Gene Craniosynostosis type 6 Genetic Test
At DNA Labs UAE, we offer the ZIC1 Gene Craniosynostosis type 6 Genetic Test for individuals who suspect they may have this condition. This test can provide valuable information about the genetic factors that contribute to craniosynostosis type 6.
Test Details
The ZIC1 gene is associated with craniosynostosis type 6, a condition characterized by the premature fusion of the skull bones. This can result in abnormal skull shape and potential neurological complications. Our NGS (Next-Generation Sequencing) genetic testing method allows us to analyze multiple genes simultaneously, including the ZIC1 gene.
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
Prior to undergoing the ZIC1 Gene Craniosynostosis type 6 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 the ZIC1 Gene Craniosynostosis type 6 NGS Genetic DNA Test gene ZIC1.
Test Process
The test involves obtaining a DNA sample, typically through a blood or saliva sample. The DNA is then sequenced using NGS technology to identify any mutations or variations in the ZIC1 gene that may be responsible for craniosynostosis type 6.
Importance of Genetic Testing
Genetic testing can play a crucial role in diagnosing craniosynostosis type 6 and providing valuable information for medical management and genetic counseling. However, it is important to undergo genetic testing under the guidance of a healthcare professional or genetic counselor. They can help interpret the test results and provide appropriate recommendations based on the individual’s specific situation.
Don’t wait any longer. Get the ZIC1 Gene Craniosynostosis type 6 Genetic Test at DNA Labs UAE and gain important insights into your genetic makeup.
| Test Name | ZIC1 Gene Craniosynostosis type 6 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 ZIC1 Gene Craniosynostosis type 6 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ZIC1 Gene Craniosynostosis type 6 NGS Genetic DNA Test gene ZIC1 |
| Test Details | The ZIC1 gene is associated with a condition called craniosynostosis type 6. Craniosynostosis is a condition characterized by the premature fusion of the skull bones, leading to abnormal skull shape and potential neurological complications. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously. In the case of craniosynostosis type 6, NGS genetic testing can identify mutations or variations in the ZIC1 gene that may be responsible for the condition. The test involves obtaining a DNA sample, typically through a blood or saliva sample, and sequencing the DNA to identify any alterations in the ZIC1 gene. This information can help in diagnosing craniosynostosis type 6 and provide valuable information for medical management and genetic counseling. It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor, who can help interpret the results and provide appropriate recommendations based on the individual’s specific situation. |
