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CDHR1 Gene Cone-Rod Dystrophy Type 15 Genetic Test

4,400 د.إ

-21%

The CDHR1 gene cone-rod dystrophy type 15 genetic test is a specialized diagnostic procedure designed to detect mutations in the CDHR1 gene, which are associated with cone-rod dystrophy type 15 (CORD15). Cone-rod dystrophy is a group of inherited eye disorders that affect the light-sensitive cells of the retina, leading to progressive vision loss. The CDHR1 gene plays a crucial role in the function and structure of these cells. Mutations in this gene can disrupt normal vision and lead to the early onset of symptoms such as decreased visual acuity, loss of color vision, and night blindness.

This test is particularly important for individuals with a family history of cone-rod dystrophy or those experiencing symptoms suggestive of the disorder. Early and accurate diagnosis through genetic testing can help in managing the condition, understanding its progression, and exploring potential treatment options.

The test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the CDHR1 gene cone-rod dystrophy type 15 genetic test is 4400 AED. It involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific mutations in the CDHR1 gene. The results of this test can provide valuable information for affected individuals and their families regarding the diagnosis, prognosis, and potential genetic counseling needs.

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CDHR1 Gene Cone-rod dystrophy type 15 Genetic Test

Welcome to DNA Labs UAE, a leading genetic lab offering the CDHR1 Gene Cone-rod dystrophy type 15 Genetic Test. This test helps in the diagnosis of cone-rod dystrophy type 15 (CORD15), a rare genetic disorder that affects the retina of the eye.

Test Details

The CDHR1 gene is associated with CORD15, which is characterized by the progressive loss of cone and rod cells in the retina, leading to vision loss and eventual blindness. Our NGS (next-generation sequencing) genetic testing method can identify mutations in the CDHR1 gene that are associated with CORD15.

Components

  • Test Name: CDHR1 Gene Cone-rod dystrophy type 15 Genetic Test
  • 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

Before undergoing the CDHR1 Gene Cone-rod dystrophy type 15 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 CDHR1 Gene Cone-rod dystrophy type 15 NGS Genetic DNA Test gene CDHR1.

Benefits of NGS Genetic Testing

NGS genetic testing is a highly accurate and efficient method for identifying genetic mutations associated with inherited disorders like CORD15. It can provide valuable information for diagnosis, prognosis, and genetic counseling for affected individuals and their families.

Conclusion

If you suspect cone-rod dystrophy type 15, our CDHR1 Gene Cone-rod dystrophy type 15 Genetic Test can help in the diagnosis and management of this condition. Our team of expert ophthalmologists and geneticists are dedicated to providing accurate and reliable genetic testing services. Contact DNA Labs UAE today to schedule your CDHR1 Gene Cone-rod dystrophy type 15 Genetic Test.

Test Name CDHR1 Gene Cone-rod dystrophy type 15 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 CDHR1 Gene Cone-rod dystrophy type 15 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CDHR1 Gene Cone-rod dystrophy type 15 NGS Genetic DNA Test gene CDHR1
Test Details

The CDHR1 gene is associated with cone-rod dystrophy type 15 (CORD15), which is a rare genetic disorder that affects the retina of the eye. This disorder is characterized by the progressive loss of cone and rod cells, leading to vision loss and eventual blindness.

NGS (next-generation sequencing) genetic testing can be used to identify mutations in the CDHR1 gene that are associated with CORD15. This test involves sequencing the entire coding region of the CDHR1 gene to identify any genetic variations that may be causing the disorder.

NGS genetic testing is a highly accurate and efficient method for identifying genetic mutations associated with inherited disorders like CORD15. It can provide valuable information for diagnosis, prognosis, and genetic counseling for affected individuals and their families.