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IFIH1 Gene Aicardi-Goutieres syndrome type 7 Genetic Test

4,400 د.إ

-21%

The IFIH1 gene plays a crucial role in the immune system, acting as a first line of defense against viral infections. Mutations in this gene can lead to Aicardi-Goutieres syndrome type 7, a rare genetic disorder characterized by severe neurological abnormalities and immune system dysfunction. This condition mimics a viral infection even in the absence of an actual virus, leading to significant brain damage and developmental issues.

To diagnose Aicardi-Goutieres syndrome type 7, a genetic test focusing on the IFIH1 gene is essential. DNA Labs UAE offers this specialized genetic testing service. The test is designed to identify mutations in the IFIH1 gene that are responsible for the syndrome, providing crucial information for diagnosis, management, and genetic counseling of affected families.

The cost of the IFIH1 Gene Aicardi-Goutieres syndrome type 7 Genetic Test at DNA Labs UAE is 4400 AED. This test is a valuable resource for families seeking answers to complex neurological and immunological symptoms presenting in their children, guiding them towards appropriate care and support strategies.

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IFIH1 Gene Aicardi-Goutieres Syndrome Type 7 Genetic Test

At DNA Labs UAE, we offer the IFIH1 Gene Aicardi-Goutieres Syndrome Type 7 Genetic Test for individuals who suspect they may have this rare genetic disorder. This test can help diagnose and manage the condition, allowing for early intervention and appropriate medical care.

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: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information

Prior to undergoing the IFIH1 Gene Aicardi-Goutieres Syndrome Type 7 Genetic Test, it is important to provide a 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 IFIH1 gene is associated with Aicardi-Goutieres Syndrome Type 7, a rare genetic disorder that affects both the brain and immune system. Individuals with this syndrome may experience neurological symptoms such as seizures, developmental delays, and intellectual disability. Additionally, immune system dysfunction can lead to inflammation in the brain and other organs.

Our NGS genetic testing method allows us to identify mutations in the IFIH1 gene that are known to cause Aicardi-Goutieres Syndrome Type 7. By sequencing the patient’s DNA, we can look for specific genetic variations associated with the syndrome.

Early diagnosis and management of Aicardi-Goutieres Syndrome Type 7 is crucial in preventing or minimizing neurological damage and other complications. Genetic testing can help identify affected individuals and their family members, enabling them to receive appropriate medical care and genetic counseling.

Test Name IFIH1 Gene Aicardi-Goutieres syndrome type 7 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 IFIH1 Gene Aicardi-Goutieres syndrome type 7 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with IFIH1 Gene Aicardi-Goutieres syndrome type 7
Test Details

The IFIH1 gene is associated with Aicardi-Goutieres syndrome type 7, which is a rare genetic disorder that affects the brain and immune system. This syndrome is characterized by neurological symptoms such as seizures, developmental delays, and intellectual disability, as well as immune system dysfunction leading to inflammation in the brain and other organs.

NGS (next-generation sequencing) genetic testing can be used to identify mutations in the IFIH1 gene that are associated with Aicardi-Goutieres syndrome type 7. This test involves sequencing the DNA of the patient to look for specific genetic variations that are known to cause the syndrome.

Early diagnosis and management of Aicardi-Goutieres syndrome type 7 is important to prevent or minimize neurological damage and other complications. Genetic testing can help identify affected individuals and their family members, allowing for appropriate medical care and genetic counseling.