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RPGRIP1 Gene Cone-Rod Dystrophy Type 13 Genetic Test

4,400 د.إ

-21%

The RPGRIP1 Gene Cone-Rod Dystrophy Type 13 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the RPGRIP1 gene that are associated with Cone-Rod Dystrophy Type 13 (CORD13). Cone-Rod Dystrophy is a group of inherited eye disorders that affect the photoreceptor cells responsible for vision, leading to a progressive loss of visual acuity, color vision, and peripheral vision. The RPGRIP1 gene plays a crucial role in the function and survival of these cells, and mutations in this gene can disrupt normal vision and lead to CORD13.

This genetic test is critical for individuals with a family history of Cone-Rod Dystrophy or those experiencing symptoms related to vision impairment, as it provides a definitive diagnosis by detecting the presence of specific genetic mutations. Early diagnosis through genetic testing can help in managing the condition, understanding the risk of passing it on to future generations, and accessing potential treatment options.

The test is conducted in the state-of-the-art facilities of DNA Labs UAE, ensuring high accuracy and reliability of results. The cost of the RPGRIP1 Gene Cone-Rod Dystrophy Type 13 Genetic Test is set at 4400 AED, reflecting the comprehensive analysis and the specialized technology employed in identifying the genetic mutations associated with this condition.

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RPGRIP1 Gene Cone-rod dystrophy type 13 Genetic Test

At DNA Labs UAE, we offer the RPGRIP1 Gene Cone-rod dystrophy type 13 Genetic Test for individuals suspected of having Cone-rod dystrophy type 13, a rare genetic disorder that affects the retina.

Test Details

The RPGRIP1 gene is associated with Cone-rod dystrophy type 13. This disorder is characterized by progressive vision loss, starting with difficulty distinguishing colors and fine details, and eventually leading to complete blindness.

Our NGS (Next-Generation Sequencing) Genetic Testing method uses advanced technology to analyze multiple genes simultaneously. This allows for a more comprehensive evaluation of an individual’s genetic makeup, providing greater accuracy and sensitivity in detecting genetic mutations associated with diseases such as Cone-rod dystrophy type 13.

If a person is suspected of having Cone-rod dystrophy type 13, a NGS Genetic Test may be recommended to identify any mutations in the RPGRIP1 gene. This information can be used to confirm a diagnosis, provide information about the inheritance pattern of the disease, and help guide treatment and management options.

Test Components and Price

Our RPGRIP1 Gene Cone-rod dystrophy type 13 Genetic Test is priced at 4400.0 AED.

The test requires a blood sample or extracted DNA, or alternatively, one drop of blood on an FTA Card.

Report Delivery

After the test is conducted, the report will be delivered within 3 to 4 weeks.

Test Type and Doctor

The RPGRIP1 Gene Cone-rod dystrophy type 13 Genetic Test falls under the category of Ophthalmology Disorders. It is recommended to consult an Ophthalmologist for this test.

Test Department

Our Genetics department handles the RPGRIP1 Gene Cone-rod dystrophy type 13 Genetic Test.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is going for the RPGRIP1 Gene Cone-rod dystrophy type 13 NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with the RPGRIP1 Gene Cone-rod dystrophy type 13 NGS Genetic DNA Test gene RPGRIP1.

Test Name RPGRIP1 Gene Cone-rod dystrophy type 13 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 RPGRIP1 Gene Cone-rod dystrophy type 13 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RPGRIP1 Gene Cone-rod dystrophy type 13 NGS Genetic DNA Test gene RPGRIP1
Test Details

The RPGRIP1 gene is associated with Cone-rod dystrophy type 13, a rare genetic disorder that affects the retina. This disorder is characterized by progressive vision loss, starting with difficulty distinguishing colors and fine details, and eventually leading to complete blindness.

NGS (Next-Generation Sequencing) Genetic Testing is a type of genetic testing that uses advanced technology to analyze multiple genes simultaneously. This allows for a more comprehensive evaluation of an individual’s genetic makeup, providing greater accuracy and sensitivity in detecting genetic mutations associated with diseases such as Cone-rod dystrophy type 13.

If a person is suspected of having Cone-rod dystrophy type 13, a NGS Genetic Test may be recommended to identify any mutations in the RPGRIP1 gene. This information can be used to confirm a diagnosis, provide information about the inheritance pattern of the disease, and help guide treatment and management options.