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MAGEL2 Gene Schaaf-Yang Syndrome Genetic Test Cost

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

-21%

The MAGEL2 Gene Schaaf-Yang Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the MAGEL2 gene, which are associated with Schaaf-Yang syndrome. This rare genetic disorder is characterized by a range of symptoms, including developmental delays, intellectual disability, muscle weakness, and distinctive facial features, among others. The test is crucial for confirming a diagnosis of Schaaf-Yang syndrome, enabling early intervention and tailored management plans for affected individuals. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately detect the specific genetic alterations linked to this condition. By choosing DNA Labs UAE for this test, patients and healthcare providers can expect reliable, accurate results that are essential for understanding and addressing the unique needs of those with Schaaf-Yang syndrome.

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MAGEL2 Gene Schaaf-Yang Syndrome Genetic Test

At DNA Labs UAE, we offer the MAGEL2 Gene Schaaf-Yang Syndrome Genetic Test. This test helps in diagnosing Schaaf-Yang syndrome, a rare genetic disorder characterized by intellectual disability, developmental delay, and various physical and behavioral features.

Test Components and Price

  • Test Name: MAGEL2 Gene Schaaf-Yang 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

Before undergoing the MAGEL2 Gene Schaaf-Yang 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 MAGEL2 Gene Schaaf-Yang Syndrome.

Test Details

The MAGEL2 gene is analyzed using NGS (Next-Generation Sequencing) technology to identify any mutations or variations that may be causing Schaaf-Yang syndrome. NGS allows for the simultaneous analysis of multiple genes, providing a comprehensive understanding of the genetic basis of the disorder.

NGS can detect small changes in the DNA sequence, such as single nucleotide variants (SNVs) or small insertions/deletions (indels), as well as larger structural variations. By analyzing the MAGEL2 gene using NGS, clinicians and researchers can determine if there are any disease-causing mutations or variations present in an individual’s DNA.

This information is crucial for diagnosis, prognosis, and potentially guiding treatment options or management strategies for individuals with Schaaf-Yang syndrome.

For more information about the MAGEL2 Gene Schaaf-Yang Syndrome Genetic Test, please contact DNA Labs UAE.

Test Name MAGEL2 Gene Schaaf-Yang 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 MAGEL2 Gene Schaaf-Yang syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MAGEL2 Gene Schaaf-Yang syndrome NGS Genetic DNA Test gene MAGEL2
Test Details

The MAGEL2 gene is associated with Schaaf-Yang syndrome, a rare genetic disorder characterized by intellectual disability, developmental delay, and a range of physical and behavioral features. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the MAGEL2 gene for mutations or variations that may be causing the syndrome.

NGS technology allows for the simultaneous analysis of multiple genes, providing a more comprehensive understanding of the genetic basis of the disorder. This type of genetic testing can identify small changes in the DNA sequence, such as single nucleotide variants (SNVs) or small insertions/deletions (indels), as well as larger structural variations.

By analyzing the MAGEL2 gene using NGS, clinicians and researchers can determine if there are any disease-causing mutations or variations present in an individual’s DNA. This information can help with diagnosis, prognosis, and potentially guide treatment options or management strategies for individuals with Schaaf-Yang syndrome.

SKU: TEST-4350 Category:

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