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PCDH15 Gene Deafness Autosomal Recessive Type 23 Genetic Test Cost

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

-21%

The PCDH15 gene plays a crucial role in the development and maintenance of hair cells in the inner ear, which are essential for hearing. Mutations in the PCDH15 gene can lead to deafness autosomal recessive type 23 (DFNB23), a form of genetic hearing loss. This condition is characterized by the absence or severe reduction of hearing from birth.

To diagnose this specific type of genetic deafness, a genetic test targeting the PCDH15 gene can be conducted. DNA Labs UAE offers this specialized test, providing a comprehensive analysis to detect mutations in the PCDH15 gene that are responsible for DFNB23. The test is priced at 4400 AED and is designed to offer crucial information for affected individuals and their families, facilitating informed decisions regarding management and potential treatment options. This genetic test is a vital tool in the early diagnosis and understanding of DFNB23, contributing to the broader efforts in addressing genetic hearing loss.

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PCDH15 Gene Deafness Autosomal Recessive Type 23 Genetic Test

Welcome to DNA Labs UAE, where we offer the PCDH15 Gene Deafness Autosomal Recessive Type 23 Genetic Test. This test is designed to identify any mutations or variations in the PCDH15 gene that may be causing deafness, specifically autosomal recessive type 23 (DFNB23).

Test Components and Price

The cost of the PCDH15 Gene Deafness Autosomal Recessive Type 23 Genetic Test is AED 4400.0. The test can be performed using blood or extracted DNA samples, or even just one drop of blood on an FTA card.

Report Delivery and Method

After the test is conducted, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology, which allows for the sequencing of multiple genes simultaneously.

Test Type and Doctor

The PCDH15 Gene Deafness Autosomal Recessive Type 23 Genetic Test falls under the category of Ear Nose Throat Disorders. It is recommended to consult with an ENT doctor for this test.

Test Department and Pre Test Information

The PCDH15 Gene Deafness Autosomal Recessive Type 23 Genetic Test is conducted in the Genetics department. Prior to the test, it is important to provide the clinical history of the patient who is going for the PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with the PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN29.

Test Details

The PCDH15 gene is associated with deafness, specifically autosomal recessive type 23 (DFNB23). This means that an individual must inherit two copies of the mutated gene (one from each parent) in order to develop the condition. The NGS genetic test involves sequencing the PCDH15 gene to identify any mutations or variations that may be causing the condition. This test can help diagnose individuals with DFNB23 and provide valuable information for genetic counseling and treatment options. It can also be used for carrier screening in individuals with a family history of DFNB23 to determine if they carry a mutated copy of the PCDH15 gene. It is important to consult with a healthcare professional or genetic counselor to discuss the specific implications and limitations of the test, as well as any potential treatment options or management strategies for individuals with PCDH15 gene deafness.

Test Name PCDH15 Gene Deafness autosomal recessive type 23 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 PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN29
Test Details

The PCDH15 gene is associated with deafness, specifically autosomal recessive type 23 (DFNB23). Autosomal recessive inheritance means that an individual must inherit two copies of the mutated gene (one from each parent) in order to develop the condition.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the sequencing of multiple genes simultaneously. In the context of PCDH15 gene deafness, an NGS genetic test would involve sequencing the PCDH15 gene to identify any mutations or variations that may be causing the condition.

This type of genetic test can help diagnose individuals with DFNB23 and provide valuable information for genetic counseling and treatment options. It can also be used for carrier screening in individuals with a family history of DFNB23 to determine if they carry a mutated copy of the PCDH15 gene.

It’s important to consult with a healthcare professional or genetic counselor to discuss the specific implications and limitations of the test, as well as any potential treatment options or management strategies for individuals with PCDH15 gene deafness.

SKU: TEST-2710 Category:

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