MED12 Gene Opitz-Kaveggia Syndrome Genetic Test
At DNA Labs UAE, we offer the MED12 Gene Opitz-Kaveggia Syndrome Genetic Test for individuals who suspect they may have this rare genetic disorder. This test can help diagnose Opitz-Kaveggia syndrome and provide valuable information about treatment options and the risk of the condition in other family members.
Test Components and Price
The MED12 Gene Opitz-Kaveggia Syndrome Genetic Test is priced at 4400.0 AED. The test analyzes the MED12 gene using Next-Generation Sequencing (NGS) technology.
Sample Condition and Report Delivery
We accept blood samples or extracted DNA for this test. Alternatively, you can provide one drop of blood on an FTA card. The report will be delivered to you within 3 to 4 weeks.
Test Method and Type
The MED12 Gene Opitz-Kaveggia Syndrome Genetic Test utilizes NGS technology to analyze the MED12 gene for mutations or variants that may be associated with Opitz-Kaveggia syndrome. This test falls under the category of dysmorphology.
Doctor and Test Department
Our experienced pediatricians handle this test, as it is commonly performed on children. The MED12 Gene Opitz-Kaveggia Syndrome Genetic Test is conducted in our Genetics department.
Pre-Test Information
Prior to undergoing the MED12 Gene Opitz-Kaveggia Syndrome Genetic 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 by Opitz-Kaveggia syndrome. This will help our geneticists interpret the test results accurately.
About Opitz-Kaveggia Syndrome and NGS Genetic Testing
Opitz-Kaveggia syndrome, also known as FG syndrome, is a rare genetic disorder that primarily affects males. It is associated with mutations or variants in the MED12 gene. NGS genetic testing allows for the simultaneous analysis of multiple genes, including MED12, enabling the identification of any abnormalities that may be present.
The MED12 Gene Opitz-Kaveggia Syndrome Genetic Test not only confirms a diagnosis but also guides treatment decisions and provides crucial information about the risk of the condition in other family members. Furthermore, it contributes to ongoing research efforts aimed at better understanding the genetic basis of Opitz-Kaveggia syndrome.
It is important to note that genetic testing for Opitz-Kaveggia syndrome should only be performed by qualified geneticists or genetic counselors who can accurately interpret the results and provide appropriate counseling and support.
| Test Name | MED12 Gene Opitz-Kaveggia syndrome 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 MED12 Gene Opitz-Kaveggia syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MED12 Gene Opitz-Kaveggia syndrome NGS Genetic DNA Test gene MED12 |
| Test Details |
The MED12 gene is associated with a genetic disorder called Opitz-Kaveggia syndrome (also known as FG syndrome). Opitz-Kaveggia syndrome is a rare genetic disorder that primarily affects males. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can be used to analyze multiple genes simultaneously. In the case of Opitz-Kaveggia syndrome, NGS genetic testing can be used to sequence the MED12 gene and identify any mutations or variants that may be present. NGS genetic testing for Opitz-Kaveggia syndrome can help confirm a diagnosis, guide treatment decisions, and provide information about the risk of the condition in other family members. It can also help researchers better understand the genetic basis of the disorder. It’s important to note that genetic testing for Opitz-Kaveggia syndrome should be performed by a qualified geneticist or genetic counselor who can interpret the results and provide appropriate counseling and support. |
