MAGT1 Gene Immunodeficiency X-Linked with Magnesium Defect Epstein-Barr Virus Infection and Neoplasia Genetic Test sale cost 4400 AED
TAC3 Gene Hypogonadotropic Hypogonadism Type 10 with or Without Anosmia Genetic Test sale cost 4400 AED TAC3 Gene Hypogonadotropic Hypogonadism Type 10 with or Without Anosmia Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
ANOS1 Gene Kallmann Syndrome Type 1 Genetic Test sale cost 4400 AED ANOS1 Gene Kallmann Syndrome Type 1 Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
Sale!

MAGT1 Gene Immunodeficiency X-Linked with Magnesium Defect Epstein-Barr Virus Infection and Neoplasia Genetic Test Cost

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

-21%

The MAGT1 Gene Immunodeficiency X-Linked with Magnesium Defect, Epstein-Barr Virus Infection, and Neoplasia Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE. This test is designed to identify mutations in the MAGT1 gene, which can lead to a rare immunodeficiency disorder. This condition is characterized by low magnesium levels, vulnerability to Epstein-Barr virus infections, and an increased risk of developing neoplasia. The MAGT1 gene plays a crucial role in magnesium ion transport within cells, and mutations can disrupt immune system function, leading to the aforementioned complications.

The test is conducted using a sample of the patient’s blood or saliva, which is then analyzed for genetic abnormalities in the MAGT1 gene. It is a vital diagnostic tool for individuals showing symptoms related to the disorder or those with a family history of the condition, as early detection can significantly impact management and treatment strategies.

DNA Labs UAE offers this comprehensive genetic test for a cost of 4400 AED. The test is performed in a state-of-the-art laboratory setting by qualified professionals, ensuring high accuracy and reliability of the results. This test is a critical step towards personalized medicine, allowing for tailored treatment plans based on the patient’s specific genetic makeup, thereby enhancing the effectiveness of treatment and improving patient outcomes.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

MAGT1 Gene Immunodeficiency X-linked with magnesium defect Epstein-Barr virus infection and neoplasia Genetic Test

Test Name: MAGT1 Gene Immunodeficiency X-linked with magnesium defect Epstein-Barr virus infection and neoplasia 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: Hepatology Nephrology Endocrinology Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for MAGT1 Gene Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MAGT1 Gene Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia NGS Genetic DNA Test gene MAGT1

Test Details: MAGT1 gene immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus (EBV) infection, and neoplasia is a rare genetic disorder. It is caused by mutations in the MAGT1 gene, which is located on the X chromosome. This condition is characterized by a range of symptoms and complications. Individuals with this disorder have impaired immune function, making them more susceptible to infections, particularly with EBV. They also have a magnesium transport defect, leading to low levels of magnesium in their cells. The most common manifestation of this condition is a severe form of EBV infection, which can cause recurrent infections, chronic active EBV infection, or even develop into lymphoma or other malignancies.

NGS genetic testing, which stands for Next-Generation Sequencing, is a type of genetic test that can be used to identify mutations in the MAGT1 gene. This test analyzes the individual’s DNA to detect any changes or abnormalities in the gene sequence. By identifying the specific mutation in the MAGT1 gene, NGS genetic testing can provide a definitive diagnosis for individuals suspected of having this disorder. It can also help determine the risk of developing complications associated with the condition.

Genetic testing is typically recommended for individuals with a family history of the disorder, those with symptoms suggestive of the condition, or those who have had recurrent or severe EBV infections. Early diagnosis through genetic testing can be beneficial in managing the condition and preventing complications. Treatment options may include antiviral medications, immune system support, and magnesium supplementation. It is important to consult with a genetic counselor or healthcare professional to discuss the benefits, limitations, and implications of genetic testing before undergoing the test.

Test Name MAGT1 Gene Immunodeficiency X-linked with magnesium defect Epstein-Barr virus infection and neoplasia 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 Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for MAGT1 Gene Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MAGT1 Gene Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia NGS Genetic DNA Test gene MAGT1
Test Details

MAGT1 gene immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus (EBV) infection, and neoplasia is a rare genetic disorder. It is caused by mutations in the MAGT1 gene, which is located on the X chromosome.

This condition is characterized by a range of symptoms and complications. Individuals with this disorder have impaired immune function, making them more susceptible to infections, particularly with EBV. They also have a magnesium transport defect, leading to low levels of magnesium in their cells.

The most common manifestation of this condition is a severe form of EBV infection, which can cause recurrent infections, chronic active EBV infection, or even develop into lymphoma or other malignancies.

NGS genetic testing, which stands for Next-Generation Sequencing, is a type of genetic test that can be used to identify mutations in the MAGT1 gene. This test analyzes the individual’s DNA to detect any changes or abnormalities in the gene sequence.

By identifying the specific mutation in the MAGT1 gene, NGS genetic testing can provide a definitive diagnosis for individuals suspected of having this disorder. It can also help determine the risk of developing complications associated with the condition.

Genetic testing is typically recommended for individuals with a family history of the disorder, those with symptoms suggestive of the condition, or those who have had recurrent or severe EBV infections.

Early diagnosis through genetic testing can be beneficial in managing the condition and preventing complications. Treatment options may include antiviral medications, immune system support, and magnesium supplementation.

It is important to consult with a genetic counselor or healthcare professional to discuss the benefits, limitations, and implications of genetic testing before undergoing the test.

SKU: TEST-3686 Category:

Related products