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FMR1 Gene Fragile X Syndrome Genetic Test

4,400 د.إ

-21%

The FMR1 Gene Fragile X Syndrome Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the FMR1 gene, which are indicative of Fragile X Syndrome (FXS). This condition is a genetic disorder that causes a range of developmental problems including learning disabilities and cognitive impairment. The test is particularly crucial for individuals with a family history of FXS or those showing symptoms of the disorder. By analyzing a sample of the individual’s DNA, the test identifies variations in the CGG repeat length within the FMR1 gene, which are responsible for causing the syndrome. The cost of the FMR1 Gene Fragile X Syndrome Genetic Test at DNA Labs UAE is 4400 AED, making it a valuable resource for families seeking answers about this inheritable condition. Early diagnosis through this test can lead to better management and support for those affected by Fragile X Syndrome.

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FMR1 Gene Fragile X syndrome Genetic Test

Cost: 4400.0 AED

Introduction

The FMR1 Gene Fragile X syndrome Genetic Test is a diagnostic test offered by DNA Labs UAE. This test analyzes the FMR1 gene for mutations that cause Fragile X syndrome, a genetic disorder that affects the X chromosome and is the most common cause of inherited intellectual disability and autism spectrum disorder.

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 (Next-Generation Sequencing)
  • Test Type: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre-Test Information

Prior to undergoing the FMR1 Gene Fragile X syndrome NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with FMR1 Gene Fragile X syndrome.

Test Details

The FMR1 gene Fragile X syndrome NGS genetic test utilizes Next-Generation Sequencing (NGS) technology to analyze the FMR1 gene for mutations associated with Fragile X syndrome. The FMR1 gene is responsible for producing a protein that is crucial for brain development and function. Mutations in this gene can lead to reduced or absent production of the protein, resulting in the symptoms of Fragile X syndrome.

This NGS genetic test is capable of detecting a variety of mutations in the FMR1 gene, including expansions of the CGG repeat sequence that are specifically linked to Fragile X syndrome. By undergoing this test, individuals can receive a diagnosis for Fragile X syndrome and gain insights into the severity of their condition.

In addition to diagnosis, this test can also be used for carrier testing in individuals with a family history of Fragile X syndrome. Furthermore, it is applicable for prenatal testing in pregnant women who are at risk of having a child with the condition.

Conclusion

The FMR1 Gene Fragile X syndrome Genetic Test offered by DNA Labs UAE is a valuable diagnostic tool for identifying mutations in the FMR1 gene that cause Fragile X syndrome. By utilizing NGS technology, this test provides accurate and comprehensive results. It is beneficial for individuals seeking a diagnosis, carrier testing, or prenatal testing. With a dedicated team of neurologists and genetics experts, DNA Labs UAE ensures reliable and efficient testing services.

Test Name FMR1 Gene Fragile X syndrome Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for FMR1 Gene Fragile X syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FMR1 Gene Fragile X syndrome
Test Details

FMR1 gene Fragile X syndrome NGS genetic test is a diagnostic test that uses Next-Generation Sequencing (NGS) technology to analyze the FMR1 gene for mutations that cause Fragile X syndrome. Fragile X syndrome is a genetic disorder that affects the X chromosome and is the most common cause of inherited intellectual disability and autism spectrum disorder. The FMR1 gene provides instructions for making a protein that is important for brain development and function. Mutations in this gene can cause the protein to be produced in lower amounts or not at all, leading to the symptoms of Fragile X syndrome. The NGS genetic test can detect a range of mutations in the FMR1 gene, including expansions of the CGG repeat sequence that are associated with Fragile X syndrome. This test can help diagnose Fragile X syndrome and provide information about the severity of the condition. It can also be used for carrier testing in individuals with a family history of Fragile X syndrome or for prenatal testing in pregnant women who are at risk of having a child with the condition.