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SAMD9 Gene Mirage Syndrome Genetic Test

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The SAMD9 Gene Mirage Syndrome Genetic Test is a sophisticated diagnostic tool available at DNA Labs UAE, designed to identify mutations in the SAMD9 gene, which are associated with Mirage Syndrome. Mirage Syndrome is a rare genetic disorder that affects various body systems, leading to a wide range of symptoms including developmental delays, growth retardation, and an increased risk of infections and certain cancers. This condition is inherited in an autosomal dominant pattern, meaning a mutation in just one copy of the gene is sufficient to cause the disorder.

The test, priced at 4400 AED, involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect mutations in the SAMD9 gene. The results from this test can provide crucial information for the diagnosis of Mirage Syndrome, enabling healthcare providers to offer appropriate treatment and management plans for affected individuals. Additionally, it can be a valuable tool for family planning and genetic counseling for families with a history of this condition. DNA Labs UAE employs state-of-the-art technology and expertise to ensure accurate and reliable testing outcomes.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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SAMD9 Gene Mirage Syndrome Genetic Test

Are you concerned about Mirage syndrome? DNA Labs UAE offers the SAMD9 Gene Mirage Syndrome Genetic Test to help diagnose this rare genetic disorder. Read on to learn more about the test, its components, cost, symptoms, and diagnosis.

Test Details

The SAMD9 gene is associated with Mirage syndrome, a rare genetic disorder characterized by growth retardation, intellectual disability, facial dysmorphism, and skeletal abnormalities. To analyze this gene, we use NGS (Next-Generation Sequencing) technology, which allows us to examine multiple genes simultaneously.

Components and Price

The SAMD9 Gene Mirage Syndrome Genetic Test costs AED 4400.0. The test requires a blood sample or extracted DNA, or just one drop of blood on an FTA Card.

Report Delivery

Once the sample is received, the report will be delivered within 3 to 4 weeks.

Test Type and Department

The SAMD9 Gene Mirage Syndrome Genetic Test falls under the category of metabolic disorders. It is conducted in our Genetics department.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who will undergo the SAMD9 Gene Mirage Syndrome NGS Genetic DNA Test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by Mirage syndrome.

Doctor and Genetic Counselor

The test will be overseen by a General Physician, who will work closely with a genetic counselor. They will guide you through the testing process, explain the potential benefits and limitations of the test, and help interpret the results.

If you suspect Mirage syndrome, consult with a healthcare professional or genetic counselor to determine if the SAMD9 Gene Mirage Syndrome Genetic Test is appropriate for you. They will provide valuable guidance and support throughout your journey.

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 Metabolic 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 Mirage syndrome
Test Details

The SAMD9 gene is associated with a rare genetic disorder called Mirage syndrome. Mirage syndrome is characterized by various symptoms, including growth retardation, intellectual disability, facial dysmorphism, and skeletal abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a diagnostic tool used to analyze multiple genes simultaneously. In the case of Mirage syndrome, NGS genetic testing can be used to identify mutations or variations in the SAMD9 gene that may be causing the disorder.

NGS testing involves sequencing the DNA of an individual to identify any genetic changes that may be present. This can help in confirming a diagnosis of Mirage syndrome and provide valuable information for genetic counseling and management of the condition.

It is important to consult with a healthcare professional or genetic counselor to determine if NGS genetic testing is appropriate for an individual suspected of having Mirage syndrome. They can provide guidance on the testing process, potential benefits, and limitations of the test, as well as help interpret the results.