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RGS9BP Gene Bradyopsia Genetic Test Cost

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

-21%

The RGS9BP Gene Bradyopsia Genetic Test is a specialized genetic assessment conducted to diagnose bradyopsia, a rare inherited eye condition characterized by a delayed adaptation of the eyes to changes in light intensity. Individuals with bradyopsia experience difficulty adjusting from brightly lit environments to darker ones, or vice versa, which can significantly impact daily activities and quality of life. The condition is linked to mutations in the RGS9BP gene, which plays a crucial role in the visual phototransduction pathway.

This genetic test involves analyzing the patient’s DNA to identify mutations in the RGS9BP gene that are responsible for bradyopsia. Early diagnosis through genetic testing can be crucial for managing symptoms and implementing strategies to cope with the visual impairment caused by this condition.

The test is available at DNA Labs UAE, a leading facility in genetic diagnostics and research. The cost of the RGS9BP Gene Bradyopsia Genetic Test is 4400 AED. This comprehensive testing service provides individuals and healthcare providers with critical information for the diagnosis and potential management of bradyopsia, enabling affected individuals to better understand their condition and live more comfortably with its implications.

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RGS9BP Gene Bradyopsia Genetic Test

Welcome to DNA Labs UAE’s blog post on the RGS9BP Gene Bradyopsia Genetic Test. In this article, we will provide you with detailed information about the test, including its components, cost, symptoms, diagnosis, and more.

Test Name: RGS9BP Gene Bradyopsia 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: Ophthalmology Disorders

Doctor: Ophthalmologist

Test Department: Genetics

Pre Test Information

Prior to undergoing the RGS9BP Gene Bradyopsia Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by the RGS9BP Gene Bradyopsia NGS Genetic DNA Test gene RGS9BP.

Test Details

The RGS9BP gene is responsible for producing a protein called RGS9-binding protein. This protein plays a crucial role in the regulation of neurotransmitters in the brain, including dopamine and serotonin. Mutations in the RGS9BP gene have been associated with various neurological disorders, including bradyopsia.

Bradyopsia is a rare condition that affects an individual’s ability to perceive visual motion. People with bradyopsia experience a delay in their perception of motion, which can lead to difficulties with activities such as driving, sports, and navigating through crowded areas. Genetic testing can be used to identify mutations in the RGS9BP gene that may be responsible for bradyopsia.

NGS (next-generation sequencing) is a state-of-the-art genetic testing technology that allows for the simultaneous analysis of multiple genes. This technology has revolutionized the field of genetics, enabling quick and accurate identification of genetic mutations associated with various disorders, including bradyopsia. NGS testing for bradyopsia typically involves sequencing the RGS9BP gene and other genes involved in visual processing.

It is important to note that genetic testing is not always necessary or appropriate for individuals with bradyopsia. A comprehensive evaluation by a healthcare professional, including a thorough eye exam and neurological assessment, may be sufficient for diagnosis and management of the condition.

If you suspect that you or a loved one may have bradyopsia or require genetic testing, we recommend consulting with an ophthalmologist or a healthcare professional specializing in genetics. They will be able to provide you with the necessary guidance and support.

Thank you for reading our blog post on the RGS9BP Gene Bradyopsia Genetic Test. For more information about our services or to schedule an appointment, please visit DNA Labs UAE’s website.

 

Test Name RGS9BP Gene Bradyopsia 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 Ophthalmology Disorders
Doctor Ophthalmologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for RGS9BP Gene Bradyopsia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RGS9BP Gene Bradyopsia NGS Genetic DNA Test gene RGS9BP
Test Details

The RGS9BP gene is responsible for producing a protein called RGS9-binding protein. This protein plays a role in the regulation of neurotransmitters in the brain, including dopamine and serotonin. Mutations in the RGS9BP gene have been associated with various neurological disorders, including bradyopsia.

Bradyopsia is a rare condition that affects the ability to perceive visual motion. People with bradyopsia experience a delay in their perception of motion, which can lead to difficulty with activities such as driving, sports, and navigating through crowded areas. Genetic testing can be used to identify mutations in the RGS9BP gene that may be responsible for bradyopsia.

NGS (next-generation sequencing) is a type of genetic testing that allows for the simultaneous analysis of multiple genes. This technology has revolutionized the field of genetics, making it possible to quickly and accurately identify genetic mutations associated with various disorders, including bradyopsia. NGS testing for bradyopsia typically involves sequencing the RGS9BP gene and other genes that may be involved in visual processing.

It is important to note that genetic testing is not always necessary or appropriate for individuals with bradyopsia. A thorough evaluation by a healthcare professional, including a comprehensive eye exam and neurological assessment, may be sufficient for diagnosis and management of the condition.