FRAS1 Gene Fraser Syndrome Genetic Test
At DNA Labs UAE, we offer the FRAS1 Gene Fraser Syndrome Genetic Test at a cost of AED 4400.0. This test is used to diagnose Fraser syndrome, a rare genetic disorder characterized by multiple birth defects affecting various parts of the body such as the eyes, ears, nose, throat, and genitalia.
Test Details
The FRAS1 gene is associated with Fraser syndrome and is inherited in an autosomal recessive manner. This means that an individual must inherit two copies of the mutated gene, one from each parent, to develop the disorder. Our Next-Generation Sequencing (NGS) technology allows us to analyze multiple genes simultaneously, including the FRAS1 gene and other genes associated with Fraser syndrome.
By performing NGS genetic testing, our healthcare professionals can identify specific mutations in the FRAS1 gene, helping to confirm a diagnosis of Fraser syndrome. This information is crucial for providing appropriate medical management and genetic counseling to affected individuals and their families.
Test Components and Price
The FRAS1 Gene Fraser Syndrome Genetic Test is performed using either blood, extracted DNA, or one drop of blood on an FTA card as a sample. The cost of this test is AED 4400.0.
Report Delivery and Method
After the test is conducted, the report will be delivered within 3 to 4 weeks. The method used for this test is NGS technology.
Test Type and Doctor
The FRAS1 Gene Fraser Syndrome Genetic Test falls under the category of Dysmorphology. It is recommended to consult with a pediatrician for this test.
Test Department
This test is conducted by our Genetics department.
Pre Test Information
Prior to undergoing the FRAS1 Gene Fraser 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 the FRAS1 Gene Fraser Syndrome NGS Genetic DNA Test gene FRAS1.
By offering this comprehensive FRAS1 Gene Fraser Syndrome Genetic Test, DNA Labs UAE aims to provide accurate diagnoses and personalized medical care to individuals and families affected by Fraser syndrome.
| Test Name | FRAS1 Gene Fraser 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 FRAS1 Gene Fraser syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FRAS1 Gene Fraser syndrome NGS Genetic DNA Test gene FRAS1 |
| Test Details |
The FRAS1 gene is associated with Fraser syndrome, which is a rare genetic disorder characterized by multiple birth defects. These defects typically affect the eyes, ears, nose, throat, and genitalia. Fraser syndrome is inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated gene (one from each parent) to develop the disorder. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the case of Fraser syndrome, NGS can be used to identify mutations in the FRAS1 gene, as well as other genes known to be associated with the disorder. By performing NGS genetic testing, healthcare professionals can identify specific mutations in the FRAS1 gene, helping to confirm a diagnosis of Fraser syndrome. This information can be useful for providing appropriate medical management and genetic counseling to affected individuals and their families. |
