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MED12 Gene Lujan-Fryns Syndrome Genetic Test Cost

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

-21%

The MED12 Gene Lujan-Fryns Syndrome Genetic Test is a specialized diagnostic examination available at DNA Labs UAE, designed to detect mutations in the MED12 gene, which are associated with Lujan-Fryns syndrome. This condition is a rare X-linked genetic disorder characterized by marfanoid habitus, intellectual disability, and distinctive facial features. The test plays a crucial role in the accurate diagnosis of the syndrome, enabling healthcare professionals to provide targeted interventions and support for affected individuals. Priced at 4400 AED, the test involves analyzing the patient’s DNA to identify specific genetic alterations in the MED12 gene, providing insights into the presence of Lujan-Fryns syndrome. This testing is essential for families seeking to understand the genetic basis of the condition, potentially guiding decisions regarding management and treatment options. DNA Labs UAE, by offering this test, contributes significantly to the field of genetic diagnostics, facilitating early detection and improved outcomes for patients with this rare genetic disorder.

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MED12 Gene Lujan-Fryns Syndrome Genetic Test

Welcome to DNA Labs UAE, where we offer the MED12 Gene Lujan-Fryns syndrome genetic test. This test can help diagnose and provide information about Lujan-Fryns syndrome, a rare genetic disorder.

Test Components

The MED12 Gene Lujan-Fryns syndrome genetic test includes the following components:

  • Test Name: MED12 Gene Lujan-Fryns syndrome Genetic Test
  • 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

Prior to undergoing the MED12 Gene Lujan-Fryns syndrome genetic test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by the syndrome.

Test Details

The MED12 gene is associated with Lujan-Fryns syndrome, a rare genetic disorder characterized by intellectual disability, behavioral problems, distinctive facial features, and other physical abnormalities. While it primarily affects males, females can also be affected with milder symptoms.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that utilizes advanced sequencing technology to analyze multiple genes simultaneously. This allows for rapid and cost-effective sequencing of large portions of the genome, including specific genes like MED12. NGS genetic testing for Lujan-Fryns syndrome involves sequencing the MED12 gene to identify any mutations or variants that may be present. This can help confirm a diagnosis and provide information about the specific genetic cause of the syndrome.

If you suspect that you or someone you know may have Lujan-Fryns syndrome, it is recommended to consult with a geneticist or healthcare professional specializing in genetics. They can provide more information about the available testing options and help determine if NGS genetic testing for the MED12 gene is appropriate for the given situation.

Test Name MED12 Gene Lujan-Fryns 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 Lujan-Fryns syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MED12 Gene Lujan-Fryns syndrome NGS Genetic DNA Test gene MED12
Test Details

The MED12 gene is associated with a condition called Lujan-Fryns syndrome. Lujan-Fryns syndrome is a rare genetic disorder characterized by intellectual disability, behavioral problems, distinctive facial features, and other physical abnormalities. It primarily affects males, although females can also be affected, albeit with milder symptoms.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. It allows for the rapid and cost-effective sequencing of large portions of the genome, including specific genes like MED12.

NGS genetic testing for Lujan-Fryns syndrome would involve sequencing the MED12 gene to identify any mutations or variants that may be present. This can help confirm a diagnosis and provide information about the specific genetic cause of the syndrome.

If you suspect that you or someone you know may have Lujan-Fryns syndrome, it is recommended to consult with a geneticist or a healthcare professional who specializes in genetics. They can provide more information about the specific testing options available and help determine if NGS genetic testing for the MED12 gene is appropriate in the given situation.

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