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SAMD9 Gene Mirage Syndrome Genetic Test

4,400 د.إ

-21%

The SAMD9 Gene Mirage Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the SAMD9 gene. These mutations are associated with MIRAGE Syndrome, a rare genetic disorder characterized by a wide range of clinical features including developmental delays, growth retardation, and various endocrine abnormalities. The test is crucial for early diagnosis and management of the syndrome, offering insights into potential treatments and interventions tailored to the patient’s genetic makeup.

Performed at the state-of-the-art facilities of DNA Labs UAE, the test involves collecting a DNA sample, typically through a blood draw, from which the SAMD9 gene is analyzed for any genetic abnormalities indicative of MIRAGE Syndrome. The cost of the test is 4400 AED, reflecting the comprehensive nature of the analysis and the sophisticated technology employed.

This genetic test is a valuable resource for families with a history of MIRAGE Syndrome or for individuals showing symptoms suggestive of the condition, providing them with essential genetic information to guide healthcare decisions.

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  • This test is not intended for medical diagnosis or treatment
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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.