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POU3F4 Gene Deafness X-Linked Type 2 Genetic Test Cost

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

-21%

The POU3F4 gene plays a critical role in the development of the inner ear, and mutations in this gene can lead to a form of hearing loss known as Deafness X-linked type 2. This condition is characterized by progressive hearing loss that mainly affects males, due to its X-linked inheritance pattern. To diagnose this specific type of genetic hearing loss, a genetic test targeting the POU3F4 gene can be conducted.

DNA Labs UAE offers a specialized genetic test for the POU3F4 gene to identify mutations associated with Deafness X-linked type 2. This test is crucial for families with a history of X-linked hearing loss, providing them with valuable information for early intervention and management strategies. The test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the lab for the presence of mutations in the POU3F4 gene.

The cost of the POU3F4 gene deafness X-linked type 2 genetic test at DNA Labs UAE is 4400 AED. This price includes the cost of sample collection, genetic analysis, and a comprehensive report that explains the test results. It is a valuable investment for affected families seeking clarity on their genetic status and guidance on managing the condition.

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POU3F4 Gene Deafness X-linked type 2 Genetic Test

Welcome to DNA Labs UAE, where we offer comprehensive genetic testing services. In this blog post, we will discuss the POU3F4 Gene Deafness X-linked type 2 Genetic Test, including its cost, symptoms, diagnosis, and more.

Test Details

The POU3F4 gene is associated with X-linked deafness type 2, a genetic condition characterized by progressive hearing loss. This condition primarily affects males and is inherited in an X-linked recessive manner. To diagnose X-linked deafness type 2, we offer an NGS (Next-Generation Sequencing) genetic test. This test involves sequencing the POU3F4 gene to identify any mutations or variations associated with the condition.

Components

  • Test Name: POU3F4 Gene Deafness X-linked type 2 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

Before undergoing the POU3F4 Gene Deafness X-linked type 2 Genetic Test, it is important to provide the clinical history of the patient who is going for the test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with the EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test gene EYA13.

Test Process

NGS testing allows for a comprehensive analysis of the POU3F4 gene, providing information on specific mutations or variations that may be present. This analysis helps in the diagnosis of X-linked deafness type 2 and can also be useful for genetic counseling and family planning purposes. It is crucial to note that genetic testing should always be performed and interpreted by a qualified healthcare professional or genetic counselor who can provide appropriate guidance and support based on the test results.

If you are interested in the POU3F4 Gene Deafness X-linked type 2 Genetic Test or have any questions, please contact DNA Labs UAE. Our team of experts is here to assist you.

Test Name POU3F4 Gene Deafness X-linked type 2 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 EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test gene EYA13
Test Details

The POU3F4 gene is associated with X-linked deafness type 2, which is a genetic condition characterized by progressive hearing loss. This condition primarily affects males, as it is inherited in an X-linked recessive manner.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of a specific gene or a panel of genes. In the case of POU3F4 gene deafness, an NGS genetic test would involve sequencing the POU3F4 gene to identify any mutations or variations that may be associated with the condition.

NGS testing allows for a comprehensive analysis of the gene, providing information on specific mutations or variations that may be present. This can help in the diagnosis of X-linked deafness type 2 and may also be useful for genetic counseling and family planning purposes.

It is important to note that genetic testing should always be performed and interpreted by a qualified healthcare professional or genetic counselor who can provide appropriate guidance and support based on the test results.

SKU: TEST-2748 Category:

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