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LYST Gene Chediak-Higashi Syndrome Genetic Test Cost

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

-21%

The LYST Gene Chediak-Higashi Syndrome Genetic Test is a specialized diagnostic procedure designed to identify mutations in the LYST gene, which are responsible for Chediak-Higashi Syndrome (CHS). CHS is a rare, autosomal recessive disorder characterized by partial albinism, immune deficiency leading to increased susceptibility to infections, and a range of other systemic problems. The test involves analyzing the patient’s DNA to detect abnormalities in the LYST gene that indicate the presence of CHS.

This genetic test is crucial for early diagnosis, allowing for appropriate management and treatment strategies to be implemented, potentially improving the quality of life for affected individuals. The test is offered at DNA Labs UAE, a reputable facility known for its comprehensive genetic testing services. The cost of the LYST Gene Chediak-Higashi Syndrome Genetic Test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately diagnose this complex condition.

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LYST Gene Chediak-Higashi Syndrome Genetic Test

At DNA Labs UAE, we offer the LYST Gene Chediak-Higashi Syndrome Genetic Test at a cost of AED 4400.0. This test is used to diagnose Chediak-Higashi syndrome (CHS), a rare genetic disorder that affects multiple systems in the body.

Test Details

The LYST gene is associated with CHS. CHS is an autosomal recessive disorder that affects the immune system and nervous system. Our Next-Generation Sequencing (NGS) technology allows for the analysis of the LYST gene to identify any mutations or variants that may be present.

Components

  • Test Name: LYST Gene Chediak-Higashi 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: Osteology Dermatology Immunology Disorders
  • Doctor: Dermatologist
  • Test Department: Genetics

Pre Test Information

Prior to the test, a Genetic Counselling session is conducted to gather the clinical history of the patient. This includes drawing a pedigree chart of family members affected with CHS and the LYST gene.

Uses of the Test

NGS genetic testing for CHS can be used to:

  • Confirm a diagnosis in individuals with suspected CHS based on their clinical symptoms.
  • Perform carrier testing in individuals with a family history of CHS.
  • Conduct prenatal testing in families at risk of having a child with CHS.

Benefits of the Test

The results of NGS genetic testing for CHS can:

  • Guide medical management and treatment decisions for individuals with CHS.
  • Provide valuable information for genetic counseling and family planning purposes.

Important Considerations

It’s important to note that NGS genetic testing may not detect all possible mutations or variants in the LYST gene. The interpretation of test results can also be challenging. Therefore, it is crucial to consult with a healthcare professional or genetic counselor who specializes in genetic testing and interpretation to fully understand the implications of the test results.

Test Name LYST Gene Chediak-Higashi 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for LYST Gene Chediak-Higashi syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LYST Gene Chediak-Higashi syndrome NGS Genetic DNA Test gene LYST
Test Details

The LYST gene is associated with a rare genetic disorder called Chediak-Higashi syndrome (CHS). CHS is an autosomal recessive disorder that affects multiple systems in the body, including the immune system and the nervous system.

Next-generation sequencing (NGS) genetic testing can be used to analyze the LYST gene and identify any mutations or variants that may be present. This type of testing allows for the simultaneous analysis of multiple genes, making it a powerful tool for diagnosing genetic disorders like CHS.

NGS genetic testing for CHS can help confirm a diagnosis in individuals with suspected CHS based on their clinical symptoms. It can also be used for carrier testing in individuals with a family history of CHS or for prenatal testing in families at risk of having a child with CHS.

The results of NGS genetic testing for CHS can help guide medical management and treatment decisions for individuals with the disorder. It can also provide valuable information for genetic counseling and family planning purposes.

It’s important to note that NGS genetic testing may not detect all possible mutations or variants in the LYST gene, and the interpretation of test results can sometimes be challenging. Therefore, it is crucial to consult with a healthcare professional or genetic counselor who specializes in genetic testing and interpretation to fully understand the implications of the test results.