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SIX1 Gene Deafness Autosomal Dominant Type 23 Genetic Test Cost

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

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The SIX1 Gene Deafness Autosomal Dominant Type 23 Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the SIX1 gene, which are linked to Autosomal Dominant Deafness Type 23 (DFNA23). This condition is characterized by varying degrees of hearing loss, often identified in early childhood or adolescence. The SIX1 gene plays a crucial role in the development of the inner ear, and mutations in this gene can disrupt normal hearing capabilities.

Conducted at DNA Labs UAE, this genetic test is pivotal for families with a history of hearing loss, providing them with crucial information regarding the genetic underpinnings of their condition. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific genetic alterations associated with DFNA23.

The cost of the SIX1 Gene Deafness Autosomal Dominant Type 23 Genetic Test is 4400 AED. This price reflects the comprehensive nature of the test, including the collection of the sample, the genetic analysis, and the provision of a detailed report that explains the results. This report is instrumental for affected individuals and their families in understanding their condition and planning for any necessary medical or supportive interventions.

DNA Labs UAE, known for its state-of-the-art facilities and highly qualified staff, ensures that the test is conducted with the highest standards of accuracy and confidentiality. The results from this test can significantly impact the management and treatment of hearing loss, offering a pathway to genetic counseling and personalized care strategies for affected individuals and their families.

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SIX1 Gene Deafness Autosomal Dominant Type 23 Genetic Test

Welcome to DNA Labs UAE, a leading genetic lab offering a wide range of genetic tests. Today, we will be discussing the SIX1 Gene Deafness Autosomal Dominant Type 23 Genetic Test, its components, cost, symptoms, diagnosis, and more.

Test Name: SIX1 Gene Deafness Autosomal Dominant Type 23 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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

If you are considering the SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 NGS Genetic DNA Test gene SLC52A4.

Test Details

The SIX1 gene is associated with autosomal dominant deafness type 23. This means that a mutation in the SIX1 gene can lead to hearing loss, and it only requires one copy of the mutated gene for the condition to be present. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the case of SIX1 gene deafness, NGS genetic testing can identify any mutations or variations in the SIX1 gene that may be causing or contributing to the hearing loss.

The NGS genetic test for SIX1 gene deafness can be helpful in diagnosing individuals with hearing loss and determining the underlying genetic cause. It can also be used for genetic counseling and family planning purposes. It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate recommendations and support.

At DNA Labs UAE, we strive to provide accurate and reliable genetic testing services. Our team of experts is dedicated to helping individuals and families understand their genetic makeup and make informed decisions regarding their health. Contact us today to learn more about the SIX1 Gene Deafness Autosomal Dominant Type 23 Genetic Test and schedule an appointment.

Test Name SIX1 Gene Deafness autosomal dominant 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 SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 NGS Genetic DNA Test gene SLC52A4
Test Details

The SIX1 gene is associated with autosomal dominant deafness type 23. This means that a mutation in the SIX1 gene can lead to hearing loss, and it only requires one copy of the mutated gene for the condition to be present.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the case of SIX1 gene deafness, NGS genetic testing can identify any mutations or variations in the SIX1 gene that may be causing or contributing to the hearing loss.

The NGS genetic test for SIX1 gene deafness can be helpful in diagnosing individuals with hearing loss and determining the underlying genetic cause. It can also be used for genetic counseling and family planning purposes.

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

SKU: TEST-2680 Category:

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