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WFS1 Gene Wolfram-Like Syndrome Autosomal Dominant Genetic Test Cost

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

-21%

The WFS1 gene is associated with Wolfram-like syndrome, a rare genetic disorder characterized by symptoms similar to Wolfram syndrome, including diabetes insipidus, diabetes mellitus, optic atrophy, and deafness, but with a less severe presentation. Unlike the classic Wolfram syndrome, which is inherited in an autosomal recessive manner, the Wolfram-like syndrome linked to mutations in the WFS1 gene follows an autosomal dominant pattern of inheritance. This means that inheriting just one copy of the mutated gene from one parent is enough to cause the disorder.

To diagnose this condition and assess the risk of passing it on to offspring, individuals suspected of having Wolfram-like syndrome or those with a family history of the disease can undergo a genetic test specifically designed to detect mutations in the WFS1 gene. One such test is available at DNA Labs UAE, a reputable facility known for its advanced genetic testing services.

The cost of the WFS1 Gene Wolfram-Like Syndrome Autosomal Dominant Genetic Test at DNA Labs UAE is 4400 AED. This test is a crucial step in confirming the diagnosis, understanding the risk for future generations, and guiding the management and treatment of affected individuals. Early diagnosis through genetic testing can lead to better management of symptoms and improved quality of life for those with Wolfram-like syndrome.

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WFS1 Gene Wolfram-like Syndrome Autosomal Dominant Genetic Test

Introduction

The WFS1 gene is associated with Wolfram-like syndrome, an autosomal dominant genetic disorder. This syndrome is characterized by various symptoms, including diabetes mellitus, optic atrophy, hearing loss, and neurological problems.

Test Details

The WFS1 Gene Wolfram-like Syndrome Autosomal Dominant Genetic Test is a specialized test offered by DNA Labs UAE. The test utilizes NGS (Next-Generation Sequencing) technology to analyze the DNA sequence of the WFS1 gene. By identifying any mutations or variations in the gene, the test can help diagnose individuals with Wolfram-like syndrome.

Components and Price

  • Test Name: WFS1 Gene Wolfram-like Syndrome Autosomal Dominant 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: Ear Nose Throat Disorders
  • Doctor: ENT Doctor
  • Test Department: Genetics
  • Pre Test Information: Clinical History of Patient going for SLC52A3 Gene Brown-Vialetto-Van Laere Syndrome 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC52A3 Gene Brown-Vialetto-Van Laere Syndrome 1 NGS Genetic DNA Test gene SLC52A22

Benefits of the Test

The WFS1 Gene Wolfram-like Syndrome Autosomal Dominant Genetic Test can provide valuable information for genetic counseling and family planning. By identifying specific mutations or variations in the WFS1 gene, the test can assist healthcare professionals in accurately diagnosing individuals with Wolfram-like syndrome. This information is crucial for providing appropriate medical care and support to affected individuals and their families.

Important Considerations

It is essential to note that genetic testing for Wolfram-like syndrome should be performed in specialized laboratories and under the guidance of a healthcare professional. The results of the genetic test should be interpreted by a geneticist or a healthcare professional with expertise in genetics to ensure accurate and meaningful information is provided to the individual and their family.

Conclusion

The WFS1 Gene Wolfram-like Syndrome Autosomal Dominant Genetic Test offered by DNA Labs UAE is a valuable tool for diagnosing individuals with Wolfram-like syndrome. By utilizing NGS technology, the test can identify mutations or variations in the WFS1 gene associated with the disorder. This information can aid in genetic counseling, family planning, and providing appropriate medical care to affected individuals.

Test Name WFS1 Gene Wolfram-like syndrome autosomal dominant 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 SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test gene SLC52A22
Test Details

The WFS1 gene is associated with Wolfram-like syndrome, which is an autosomal dominant genetic disorder. This disorder is characterized by a combination of various symptoms including diabetes mellitus, optic atrophy (degeneration of the optic nerve), hearing loss, and neurological problems.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of genes. In the context of WFS1 gene testing, NGS can be used to identify any mutations or variations in the WFS1 gene that may be causing or contributing to the development of Wolfram-like syndrome.

By analyzing the DNA sequence of the WFS1 gene, NGS can detect specific mutations or variations that may be associated with the disorder. This information can help in diagnosing individuals with Wolfram-like syndrome and also provide valuable information for genetic counseling and family planning.

It is important to note that genetic testing for Wolfram-like syndrome is typically performed in specialized laboratories and requires a healthcare professional’s involvement. The results of the genetic test should be interpreted by a geneticist or a healthcare professional with expertise in genetics to provide accurate and meaningful information to the individual and their family.