SAMD9 Gene Mirage Syndrome Genetic Test
Welcome to DNA Labs UAE, your trusted genetic testing laboratory. We offer the SAMD9 Gene Mirage Syndrome Genetic Test at a cost of AED 4400.0.
Test Components and Price
The SAMD9 Gene Mirage Syndrome Genetic Test includes:
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test Type: Hepatology Nephrology Endocrinology Disorders
- Doctor: General Physician
- Test Department: Genetics
The cost of the test is AED 4400.0.
Test Details
The SAMD9 Gene Mirage Syndrome Genetic Test is a diagnostic test that utilizes next-generation sequencing (NGS) technology to analyze the SAMD9 gene for mutations or variations associated with Mirage syndrome. Mirage syndrome is a rare genetic disorder characterized by intellectual disability, developmental delay, growth abnormalities, distinctive facial features, and other physical abnormalities.
The NGS technology enables the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic variations potentially responsible for the syndrome. This test is particularly useful in confirming a diagnosis of Mirage syndrome in individuals exhibiting symptoms associated with the condition.
To perform the test, a blood or saliva sample is collected from the individual being tested. The sample is then sent to our laboratory where the DNA is extracted and analyzed using NGS technology.
Pre-Test Information
Before undergoing the SAMD9 Gene Mirage Syndrome Genetic Test, it is essential to provide the clinical history of the patient who will be tested. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by the SAMD9 Gene Mirage Syndrome NGS Genetic DNA Test gene SAMD9.
Test Benefits
The results of the SAMD9 Gene Mirage Syndrome Genetic Test can:
- Guide medical management
- Provide information on recurrence risks
- Inform genetic counseling
It is important to note that this test is typically ordered by healthcare professionals specializing in genetics or genetic counseling. The test results should be interpreted in conjunction with the individual’s clinical presentation and family history to ensure an accurate diagnosis and appropriate management.
Test Name | SAMD9 Gene Mirage 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 | Hepatology Nephrology Endocrinology Disorders |
Doctor | General Physician |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for SAMD9 Gene Mirage syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SAMD9 Gene Mirage syndrome NGS Genetic DNA Test gene SAMD9 |
Test Details |
The SAMD9 gene Mirage syndrome NGS genetic test is a diagnostic test that uses next-generation sequencing (NGS) technology to analyze the SAMD9 gene for mutations or variations that may be associated with Mirage syndrome. Mirage syndrome is a rare genetic disorder characterized by intellectual disability, developmental delay, growth abnormalities, distinctive facial features, and other physical abnormalities. The NGS technology allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic variations that may be responsible for the syndrome. This test can help confirm a diagnosis of Mirage syndrome in individuals who exhibit symptoms associated with the condition. The test involves collecting a blood or saliva sample from the individual being tested. The sample is then sent to a laboratory where the DNA is extracted and analyzed using NGS technology. The results of the test can help guide medical management, provide information on recurrence risks, and potentially inform genetic counseling. It is important to note that this test is typically ordered by healthcare professionals who specialize in genetics or genetic counseling. The test results should be interpreted in conjunction with the individual’s clinical presentation and family history to ensure accurate diagnosis and appropriate management. |