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SERPINB6 Gene Deafness Autosomal Recessive Type 91 Genetic Test

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

-21%

The SERPINB6 gene, associated with Autosomal Recessive Deafness Type 91 (DFNB91), plays a critical role in the function and maintenance of the inner ear’s structure. Mutations in this gene can lead to hearing loss, which is typically present from birth. The condition follows an autosomal recessive inheritance pattern, meaning that an individual must inherit two copies of the mutated gene (one from each parent) to exhibit symptoms of the disorder.

To diagnose this specific type of genetic hearing loss, DNA Labs UAE offers a genetic test targeting the SERPINB6 gene. This test is essential for individuals with a family history of hearing loss or parents who are potential carriers of the mutation and wish to assess their children’s risk. The procedure involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed for mutations in the SERPINB6 gene.

The cost of the SERPINB6 Gene Deafness Autosomal Recessive Type 91 Genetic Test at DNA Labs UAE is 4400 AED. This test is a valuable tool for early detection and management of hearing loss, allowing families to make informed decisions regarding their health and any necessary interventions.

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SERPINB6 Gene Deafness Autosomal Recessive Type 91 Genetic Test

At DNA Labs UAE, we offer the SERPINB6 Gene Deafness Autosomal Recessive Type 91 Genetic Test. This test is designed to detect genetic variations or mutations in the SERPINB6 gene that may be associated with a type of deafness known as autosomal recessive type 91 (DFNB91).

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

Prior to undergoing the SERPINB6 Gene Deafness Autosomal Recessive Type 91 Genetic Test, it is important to provide the clinical history of the patient who is also going for the SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test. A genetic counseling session will be conducted to draw a pedigree chart of family members affected with SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test gene SLC52A14.

Test Details

The SERPINB6 gene is associated with autosomal recessive type 91 (DFNB91) deafness, which is characterized by profound hearing loss present from birth. Our NGS (Next-Generation Sequencing) genetic testing method allows for the simultaneous analysis of multiple genes to identify genetic variations or mutations related to specific conditions. In the case of DFNB91, NGS testing can help identify mutations in the SERPINB6 gene that may be causing the deafness.

By identifying the specific genetic mutation causing DFNB91, the NGS test provides crucial information for diagnosis, prognosis, and potential treatment options. Additionally, it aids in genetic counseling by determining the risk of passing on the condition to future generations.

It is essential to consult with a healthcare professional or genetic counselor to fully understand the implications and limitations of NGS testing for SERPINB6 gene deafness, autosomal recessive type 91.

Test Name SERPINB6 Gene Deafness autosomal recessive type 91 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 SLC52A14
Test Details

The SERPINB6 gene is associated with a type of deafness known as autosomal recessive type 91 (DFNB91). This genetic condition is characterized by profound hearing loss that is present from birth.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations that may be associated with a particular condition. In the case of DFNB91, NGS genetic testing can be used to identify mutations in the SERPINB6 gene that may be causing the deafness.

By identifying the specific genetic mutation causing DFNB91, NGS testing can provide important information for diagnosis, prognosis, and potential treatment options. It can also help in genetic counseling by determining the risk of passing on the condition to future generations.

It’s important to consult with a healthcare professional or genetic counselor to discuss the specific implications and limitations of NGS testing for SERPINB6 gene deafness, autosomal recessive type 91.

SKU: TEST-2742 Category:

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