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RNASEH2C Gene Aicardi-Goutieres syndrome type 3 Genetic Test

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

-21%

The RNASEH2C gene plays a critical role in the development of Aicardi-Goutieres syndrome type 3, a rare genetic disorder characterized by neurological and immunological abnormalities. Aicardi-Goutieres syndrome can mimic congenital viral infections and leads to a range of symptoms, including developmental delay, microcephaly, and skin lesions, among others. It is an autosomal recessive condition, meaning that an affected individual inherits two defective copies of the gene, one from each parent.

Genetic testing for mutations in the RNASEH2C gene is essential for the accurate diagnosis of Aicardi-Goutieres syndrome type 3. This test involves analyzing the DNA to identify mutations in the RNASEH2C gene that are known to cause the disorder. Early diagnosis through genetic testing can aid in the management of the condition and help inform family planning decisions.

In the UAE, this specific genetic test is available at DNA Labs UAE, a reputable facility known for its comprehensive range of genetic testing services. The cost of the RNASEH2C gene test for Aicardi-Goutieres syndrome type 3 is 4400 AED. This test is crucial for families with a history of the syndrome or who have children showing symptoms indicative of the condition. By opting for this test, parents can gain valuable insights into their child’s health and make informed decisions about their care and treatment options.

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RNASEH2C Gene Aicardi-Goutieres Syndrome Type 3 Genetic Test

Introduction

The RNASEH2C gene is associated with Aicardi-Goutieres syndrome type 3, a rare genetic disorder that affects the brain and immune system. DNA Labs UAE offers a NGS genetic test to analyze the RNASEH2C gene and detect mutations or variants that may cause Aicardi-Goutieres syndrome type 3.

Test Components and Price

  • Test Name: RNASEH2C Gene Aicardi-Goutieres syndrome type 3 Genetic Test
  • Components: NGS Technology
  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Test Type: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Before undergoing the RNASEH2C Gene Aicardi-Goutieres syndrome type 3 NGS Genetic DNA 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 with RNASEH2C Gene Aicardi-Goutieres syndrome type 3.

Test Details

The RNASEH2C Gene Aicardi-Goutieres syndrome type 3 Genetic Test involves sequencing the DNA of the patient and comparing it to a reference genome to identify any genetic changes that may be responsible for the disorder. The results of the test can help diagnose Aicardi-Goutieres syndrome type 3 and provide information for genetic counseling and management of the condition.

Test Name RNASEH2C Gene Aicardi-Goutieres syndrome type 3 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 RNASEH2C Gene Aicardi-Goutieres syndrome type 3 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with RNASEH2C Gene Aicardi-Goutieres syndrome type 3
Test Details

The RNASEH2C gene is associated with Aicardi-Goutieres syndrome type 3, a rare genetic disorder that affects the brain and immune system. A NGS genetic test can be used to analyze the RNASEH2C gene and detect mutations or variants that may cause Aicardi-Goutieres syndrome type 3. This test involves sequencing the DNA of the patient and comparing it to a reference genome to identify any genetic changes that may be responsible for the disorder. Results of the test can help diagnose Aicardi-Goutieres syndrome type 3 and provide information for genetic counseling and management of the condition.