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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 plays a crucial role in cellular stress response, particularly in the endoplasmic reticulum. Mutations in this gene are responsible for Wolcott-Rallison syndrome, a rare autosomal recessive disorder characterized by early-onset diabetes, skeletal dysplasia, and, in some cases, multiple organ dysfunction. Given the genetic basis of this condition, genetic testing is essential for accurate diagnosis, carrier testing, and prenatal diagnosis.

DNA Labs UAE offers a comprehensive genetic test targeting the EIF2AK3 gene to diagnose Wolcott-Rallison syndrome. The test involves analyzing the patient’s DNA to identify mutations in the EIF2AK3 gene that are indicative of the syndrome. This test is crucial for families with a history of the condition, individuals showing symptoms, or couples considering pregnancy who may be at risk.

The cost of the EIF2AK3 gene genetic test at DNA Labs UAE is 4400 AED. The test is conducted with high precision, utilizing advanced genetic sequencing technologies to ensure accurate results. Once the test is completed, a detailed report is provided, offering insights into the patient’s genetic status concerning the EIF2AK3 gene. This information is invaluable for guiding clinical decisions, including management and treatment options for affected individuals.

In summary, the EIF2AK3 gene genetic test offered by DNA Labs UAE is a vital tool in the diagnosis and management of Wolcott-Rallison syndrome, providing crucial genetic insights for affected families at the cost of 4400 AED.

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EIF2AK3 Gene Wolcott-Rallison Syndrome Genetic Test

Welcome to DNA Labs UAE, a leading genetic lab offering the EIF2AK3 Gene Wolcott-Rallison Syndrome Genetic Test. In this blog, we will discuss the cost, symptoms, diagnosis, and other important details related to this 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

Hepatology Nephrology Endocrinology Disorders

Doctor

General Physician

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 responsible for producing a protein called eukaryotic translation initiation factor 2-alpha kinase 3. Mutations in this gene can lead to a rare autosomal recessive disorder known as Wolcott-Rallison Syndrome (WRS). Wolcott-Rallison Syndrome is characterized by early-onset diabetes mellitus, multiple epiphyseal dysplasia, and hepatic dysfunction. It is a rare condition, with less than 100 cases reported worldwide.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or the entire genome. In the case of Wolcott-Rallison Syndrome, NGS can be used to identify mutations in the EIF2AK3 gene that are associated with the condition. NGS genetic testing involves sequencing the DNA of an individual to identify any variations or mutations in specific genes. This can help in the diagnosis of genetic disorders, such as Wolcott-Rallison Syndrome, and provide valuable information for treatment and management of the condition.

It is important to consult with a healthcare professional or a genetic counselor to discuss the benefits, limitations, and potential risks of genetic testing before undergoing the test. They can also provide guidance on the interpretation of the test results and any necessary follow-up steps.

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 Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
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 responsible for producing a protein called eukaryotic translation initiation factor 2-alpha kinase 3. Mutations in this gene can lead to a rare autosomal recessive disorder known as Wolcott-Rallison syndrome (WRS).

Wolcott-Rallison syndrome is characterized by early-onset diabetes mellitus, multiple epiphyseal dysplasia, and hepatic dysfunction. It is a rare condition, with less than 100 cases reported worldwide.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or the entire genome. In the case of Wolcott-Rallison syndrome, NGS can be used to identify mutations in the EIF2AK3 gene that are associated with the condition.

NGS genetic testing involves sequencing the DNA of an individual to identify any variations or mutations in specific genes. This can help in the diagnosis of genetic disorders, such as Wolcott-Rallison syndrome, and provide valuable information for treatment and management of the condition.

It is important to consult with a healthcare professional or a genetic counselor to discuss the benefits, limitations, and potential risks of genetic testing before undergoing the test. They can also provide guidance on the interpretation of the test results and any necessary follow-up steps.

SKU: TEST-3809 Category:

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