WFS1 Gene Wolfram Syndrome Type 1 Genetic Test sale cost 4400 AED
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WFS1 Gene Wolfram Syndrome Type 1 Genetic Test Cost

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

-21%

The WFS1 Gene Wolfram Syndrome Type 1 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the WFS1 gene, which are indicative of Wolfram Syndrome Type 1. This rare, genetic disorder is characterized by diabetes insipidus, diabetes mellitus, optic atrophy, and deafness, collectively known as DIDMOAD. The test is crucial for individuals showing symptoms of the syndrome or those with a family history of the condition, as it provides essential information for diagnosis, management, and genetic counseling. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately detect the specific gene mutations associated with this condition. Conducted in the state-of-the-art facilities of DNA Labs UAE, this test represents a significant step forward in the personalized care and management of patients with Wolfram Syndrome Type 1.

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WFS1 Gene Wolfram syndrome type 1 Genetic Test

At DNA Labs UAE, we offer the WFS1 Gene Wolfram syndrome type 1 Genetic Test at a cost of AED 4400.0. This test is used to diagnose Wolfram syndrome type 1, a rare genetic disorder characterized by various symptoms such as diabetes mellitus, optic atrophy, hearing loss, and neurological abnormalities.

Test Details

The WFS1 gene is associated with Wolfram syndrome type 1. Our Next-Generation Sequencing (NGS) technology allows for the simultaneous analysis of multiple genes, including the WFS1 gene, to identify any variations or mutations that may be present. This test can confirm a diagnosis of Wolfram syndrome type 1 by detecting mutations in the WFS1 gene.

In addition to diagnosis, the test can also be used for carrier testing and to provide information about the risk of passing on the condition to future generations.

Test Components and Price

The WFS1 Gene Wolfram syndrome type 1 Genetic Test is priced at AED 4400.0. The test requires a blood or extracted DNA sample, or one drop of blood on an FTA card.

Report Delivery

The report will be delivered within 3 to 4 weeks.

Test Method

The test utilizes NGS technology for analysis.

Test Type

The test is specifically designed for Ear Nose Throat Disorders and is recommended by ENT doctors.

Test Department

The test is conducted by our Genetics department.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is going for the GJB2 Gene Deafness with keratopachydermia and constrictions of fingers and toes NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with GJB2 Gene Deafness with keratopachydermia and constrictions of fingers and toes NGS Genetic DNA Test gene GJB20.

This pre-test information helps us gather important data to ensure accurate results.

At DNA Labs UAE, we strive to provide comprehensive genetic testing services to help healthcare providers make informed decisions about treatment and management options for individuals with Wolfram syndrome type 1. Our NGS genetic testing method ensures accurate and reliable results.

Test Name WFS1 Gene Wolfram 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 Ear Nose Throat Disorders
Doctor ENT Doctor
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for GJB2 Gene Deafness with keratopachydermia and constrictions of fingers and toes NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GJB2 Gene Deafness with keratopachydermia and constrictions of fingers and toes NGS Genetic DNA Test gene GJB20
Test Details

The WFS1 gene is associated with Wolfram syndrome type 1, a rare genetic disorder characterized by the development of multiple symptoms including diabetes mellitus, optic atrophy (leading to vision loss), hearing loss, and neurological abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the WFS1 gene, to identify any variations or mutations that may be present. This test can help confirm a diagnosis of Wolfram syndrome type 1 by detecting mutations in the WFS1 gene. It can also be used for carrier testing or to provide information about the risk of passing on the condition to future generations.

NGS genetic testing typically involves obtaining a DNA sample, usually through a blood or saliva sample, and analyzing it in a laboratory using advanced sequencing technology. The results of the test can help healthcare providers make informed decisions about treatment and management options for individuals with Wolfram syndrome type 1.

SKU: TEST-2796 Category:

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