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MYO5A Gene Griscelli syndrome type 1 Genetic Test Cost

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

-21%

The MYO5A gene plays a crucial role in the development and function of various cells within the body, including those involved with pigmentation and immune response. Mutations in the MYO5A gene are responsible for Griscelli syndrome type 1, a rare genetic disorder characterized by pigmentary dilution of the skin and hair, leading to a silvery-gray sheen, and neurological problems without immunodeficiency. This condition is inherited in an autosomal recessive pattern.

To diagnose this specific type of Griscelli syndrome, a genetic test targeting the MYO5A gene can be conducted. DNA Labs UAE offers this specialized genetic testing service. The test is designed to identify mutations in the MYO5A gene that are indicative of Griscelli syndrome type 1. It is a critical tool for accurate diagnosis, allowing for appropriate management and care of affected individuals.

The cost of the MYO5A gene Griscelli syndrome type 1 genetic test at DNA Labs UAE is 4400 AED. This test is an important step for families seeking answers to unexplained symptoms related to pigmentation and neurological issues, providing them with crucial information for genetic counseling and understanding the risk for future offspring.

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MYO5A Gene Griscelli syndrome type 1 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 MYO5A Gene Griscelli syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MYO5A Gene Griscelli syndrome type 1 NGS Genetic DNA Test gene MYO5A.

Test Details:

The MYO5A gene is associated with Griscelli syndrome type 1, a rare genetic disorder characterized by pigmentary dilution of the skin and hair, immunodeficiency, and neurological abnormalities. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the detection of genetic variations or mutations that may be associated with a particular disorder. In the case of Griscelli syndrome type 1, NGS genetic testing can be used to identify variations or mutations in the MYO5A gene that may be causing the disorder.

NGS genetic testing involves sequencing the DNA of an individual to identify any changes or mutations in specific genes. This can help in confirming a diagnosis, providing information about the genetic cause of the disorder, and guiding treatment options and genetic counseling. It is important to consult with a genetic counselor or healthcare professional to discuss the appropriateness and availability of NGS genetic testing for Griscelli syndrome type 1 and to understand the implications of the test results.

Test Name MYO5A Gene Griscelli syndrome type 1 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 MYO5A Gene Griscelli syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MYO5A Gene Griscelli syndrome type 1 NGS Genetic DNA Test gene MYO5A
Test Details

The MYO5A gene is associated with Griscelli syndrome type 1, a rare genetic disorder characterized by pigmentary dilution of the skin and hair, immunodeficiency, and neurological abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the detection of genetic variations or mutations that may be associated with a particular disorder. In the case of Griscelli syndrome type 1, NGS genetic testing can be used to identify variations or mutations in the MYO5A gene that may be causing the disorder.

NGS genetic testing involves sequencing the DNA of an individual to identify any changes or mutations in specific genes. This can help in confirming a diagnosis, providing information about the genetic cause of the disorder, and guiding treatment options and genetic counseling.

It is important to consult with a genetic counselor or healthcare professional to discuss the appropriateness and availability of NGS genetic testing for Griscelli syndrome type 1 and to understand the implications of the test results.

SKU: TEST-3009 Category:

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