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.
| 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. |
