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EIF2AK3 Gene Wolcott-Rallison Syndrome Genetic Test Cost

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

-21%

The EIF2AK3 Gene Wolcott-Rallison Syndrome Genetic Test is a specialized diagnostic examination designed to identify mutations in the EIF2AK3 gene, which are associated with Wolcott-Rallison Syndrome (WRS). WRS is a rare autosomal recessive disorder characterized by early-onset diabetes, skeletal dysplasia, and, in some cases, multiple organ dysfunction. This genetic test is crucial for confirming the diagnosis of WRS, enabling appropriate management and genetic counseling for affected individuals and their families.

Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, typically through a blood draw, from the patient. The laboratory then uses advanced genomic sequencing technologies to analyze the EIF2AK3 gene for any mutations known to cause Wolcott-Rallison Syndrome. The cost of the EIF2AK3 Gene Wolcott-Rallison Syndrome Genetic Test at DNA Labs UAE is 4400 AED.

This test is particularly important for individuals showing symptoms of WRS or those with a family history of the disorder, as early detection can significantly influence the management of the condition. Given the complexity of Wolcott-Rallison Syndrome and its implications for affected individuals, this genetic test is a valuable tool in the diagnostic process.

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EIF2AK3 Gene Wolcott-Rallison Syndrome Genetic Test

At DNA Labs UAE, we offer the EIF2AK3 Gene Wolcott-Rallison Syndrome Genetic Test at a cost of AED 4400.0. This test is designed to diagnose Wolcott-Rallison syndrome, a rare genetic disorder associated with the EIF2AK3 gene.

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 and Test Department

This test is performed by a dermatologist in our Genetics department.

Pre Test Information

Prior to undergoing the EIF2AK3 Gene Wolcott-Rallison Syndrome NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the syndrome.

Test Details

The EIF2AK3 gene is associated with Wolcott-Rallison syndrome, which is characterized by early-onset diabetes, multiple organ failure, and skeletal abnormalities. Our NGS genetic testing method allows for the simultaneous analysis of multiple genes to identify genetic variations or mutations related to this syndrome.

NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome to detect any genetic variations or mutations. This test specifically focuses on identifying mutations in the EIF2AK3 gene.

Important Considerations

It is crucial to note that NGS genetic testing should be conducted by specialized laboratories and under the order of a healthcare professional. The results of the test should be interpreted by a geneticist or genetic counselor who can provide appropriate guidance and support.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Contact us today to schedule an appointment for the EIF2AK3 Gene Wolcott-Rallison Syndrome Genetic Test.

Test Name EIF2AK3 Gene Wolcott-Rallison 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 EIF2AK3 Gene Wolcott-Rallison syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EIF2AK3 Gene Wolcott-Rallison syndrome NGS Genetic DNA Test gene EIF2AK3
Test Details

The EIF2AK3 gene is associated with a rare genetic disorder called Wolcott-Rallison syndrome (WRS). WRS is characterized by early-onset diabetes, multiple organ failure, and skeletal abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations that may be associated with a particular disorder or condition. In the case of Wolcott-Rallison syndrome, NGS genetic testing can be used to detect mutations in the EIF2AK3 gene, which is known to cause this syndrome.

NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome to identify any genetic variations or mutations. This can help in the diagnosis of Wolcott-Rallison syndrome and provide valuable information for patient management and genetic counseling.

It is important to note that NGS genetic testing is typically performed by specialized laboratories and requires a healthcare professional’s order. The test results should be interpreted by a geneticist or genetic counselor who can provide appropriate guidance and support.