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RDX Gene Deafness Autosomal Recessive Type 24 Genetic Test Cost

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

-21%

The RDX Gene Deafness Autosomal Recessive Type 24 Genetic Test is a specialized diagnostic procedure designed to identify mutations in the RDX gene, which are linked to a specific type of hereditary hearing loss known as Autosomal Recessive Deafness Type 24 (DFNB24). This form of hearing impairment is passed down through families in an autosomal recessive pattern, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected.

The test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The process involves collecting a DNA sample from the patient, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect any genetic abnormalities associated with the RDX gene.

The cost of the RDX Gene Deafness Autosomal Recessive Type 24 Genetic Test at DNA Labs UAE is set at 4400 AED. This price includes the comprehensive analysis required to accurately identify the presence of the specific gene mutations linked to this type of deafness. For individuals with a family history of hearing loss or parents planning to have children and wanting to assess their genetic risk, this test provides crucial information that can help in managing or mitigating the impact of this condition.

By pinpointing the genetic cause of hearing loss, the test not only facilitates early intervention and treatment options but also offers valuable insights for family planning and genetic counseling, aiding families in understanding their genetic makeup and its implications for future generations.

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RDX Gene Deafness Autosomal Recessive Type 24 Genetic Test

At DNA Labs UAE, we offer the RDX Gene Deafness Autosomal Recessive Type 24 Genetic Test. This test helps in diagnosing a specific type of genetic deafness that is inherited in an autosomal recessive manner.

Test Details

RDX gene deafness, autosomal recessive type 24 is a specific type of genetic deafness that is inherited in an autosomal recessive manner. This means that an individual must inherit two copies of the mutated RDX gene, one from each parent, in order to develop the condition.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of RDX gene deafness, autosomal recessive type 24, NGS genetic testing would involve sequencing the RDX gene to identify any mutations or variants that may be associated with the condition.

NGS genetic testing can provide valuable information about an individual’s genetic makeup and help in diagnosing genetic disorders, including RDX gene deafness, autosomal recessive type 24. It can also be used for carrier testing to determine if an individual carries a mutated gene associated with the condition, even if they do not show any symptoms themselves.

It is important to consult with a healthcare professional or genetic counselor to understand the implications of genetic testing and to interpret the results accurately. They can provide guidance on the appropriate testing options, potential risks, and the available support and treatment options for individuals with RDX gene deafness, autosomal recessive type 24.

Test Components and Price

  • Test Name: RDX Gene Deafness Autosomal Recessive Type 24 Genetic Test
  • Components: NGS Technology
  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Test Type: Ear Nose Throat Disorders
  • Doctor: ENT Doctor
  • Test Department: Genetics

Pre Test Information

Before undergoing the RDX Gene Deafness Autosomal Recessive Type 24 Genetic Test, it is important to provide the clinical history of the patient who is going for CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test. A Genetic Counselling session may be conducted to draw a pedigree chart of family members affected with CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test gene CATSPER8.

Ensure to consult with a healthcare professional or genetic counselor to gather all the necessary information and understand the testing process.

Test Name RDX Gene Deafness autosomal recessive type 24 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 CATSPER8
Test Details

RDX gene deafness, autosomal recessive type 24 is a specific type of genetic deafness that is inherited in an autosomal recessive manner. This means that an individual must inherit two copies of the mutated RDX gene, one from each parent, in order to develop the condition.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of RDX gene deafness, autosomal recessive type 24, NGS genetic testing would involve sequencing the RDX gene to identify any mutations or variants that may be associated with the condition.

NGS genetic testing can provide valuable information about an individual’s genetic makeup and help in diagnosing genetic disorders, including RDX gene deafness, autosomal recessive type 24. It can also be used for carrier testing to determine if an individual carries a mutated gene associated with the condition, even if they do not show any symptoms themselves.

It is important to consult with a healthcare professional or genetic counselor to understand the implications of genetic testing and to interpret the results accurately. They can provide guidance on the appropriate testing options, potential risks, and the available support and treatment options for individuals with RDX gene deafness, autosomal recessive type 24.