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POU4F3 Gene Deafness Autosomal Dominant Type 15 Genetic Test

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

-21%

The POU4F3 gene is associated with Autosomal Dominant Deafness Type 15 (DFNA15), a genetic condition that affects hearing. The POU4F3 gene plays a crucial role in the development and maintenance of hair cells in the inner ear, which are essential for normal hearing. Mutations in the POU4F3 gene can lead to progressive hearing loss, typically starting in late childhood or early adulthood.

To diagnose this specific type of genetic deafness, DNA Labs UAE offers a genetic test targeting the POU4F3 gene. This test is designed to identify mutations in the POU4F3 gene that are responsible for Autosomal Dominant Deafness Type 15. Early identification of these mutations can be beneficial for affected individuals and their families for several reasons, including understanding the cause of the hearing loss, exploring potential treatment options, and making informed decisions about family planning.

The cost of the POU4F3 Gene Deafness Autosomal Dominant Type 15 Genetic Test at DNA Labs UAE is 4400 AED. This investment includes the collection of a DNA sample, usually through a blood draw or cheek swab, and comprehensive analysis to detect any mutations in the POU4F3 gene. Results from this test can provide valuable information for managing and treating hearing loss associated with DFNA15.

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POU4F3 Gene Deafness Autosomal Dominant Type 15 Genetic Test

Cost: AED 4400.0

Test Details

The POU4F3 gene is associated with autosomal dominant deafness type 15. Autosomal dominant means that only one copy of the mutated gene is needed to cause the condition. NGS (Next Generation Sequencing) is a genetic testing method that allows for the simultaneous sequencing of multiple genes or even the entire genome. In the case of POU4F3 gene deafness, NGS can be used to analyze the DNA sequence of the POU4F3 gene and identify any mutations or variations that may be causing the condition.

NGS genetic testing for POU4F3 gene deafness can be used to diagnose individuals with the condition, determine the specific genetic cause of their deafness, and provide information about the inheritance pattern for their family members. This information can be helpful for genetic counseling, family planning, and potentially guiding treatment options in the future.

It’s important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate support and guidance.

Test Components

  • Price: AED 4400.0
  • 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 CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test gene CATSPER3.

Test Name POU4F3 Gene Deafness autosomal dominant type 15 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 CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test gene CATSPER3
Test Details

The POU4F3 gene is associated with autosomal dominant deafness type 15. Autosomal dominant means that only one copy of the mutated gene is needed to cause the condition.

NGS (Next Generation Sequencing) is a genetic testing method that allows for the simultaneous sequencing of multiple genes or even the entire genome. In the case of POU4F3 gene deafness, NGS can be used to analyze the DNA sequence of the POU4F3 gene and identify any mutations or variations that may be causing the condition.

NGS genetic testing for POU4F3 gene deafness can be used to diagnose individuals with the condition, determine the specific genetic cause of their deafness, and provide information about the inheritance pattern for their family members. This information can be helpful for genetic counseling, family planning, and potentially guiding treatment options in the future.

It’s important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate support and guidance.

SKU: TEST-2676 Category:

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