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CNGB3 Gene Achromatopsia Type 3 Genetic Test

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

-21%

The CNGB3 gene achromatopsia type 3 genetic test is a specialized diagnostic tool designed to identify mutations in the CNGB3 gene, which are known to cause achromatopsia type 3. Achromatopsia is a rare, inherited eye condition characterized by partial or total absence of color vision, light sensitivity, and reduced visual acuity. This condition results from mutations in several genes, including CNGB3, which plays a critical role in the normal functioning of cone cells in the retina responsible for color vision.

The test involves collecting a DNA sample, typically through a blood draw or cheek swab, and analyzing it for specific genetic alterations in the CNGB3 gene. Identifying these mutations can confirm a diagnosis of achromatopsia type 3, allowing for appropriate management and genetic counseling for affected individuals and their families.

This genetic test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the CNGB3 gene achromatopsia type 3 genetic test is 4400 AED. This investment in genetic testing can be crucial for families seeking answers about this condition, as it not only aids in diagnosis but also helps in understanding the inheritance pattern, potential risks to other family members, and considerations for future pregnancies.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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CNGB3 Gene Achromatopsia type 3 Genetic Test

At DNA Labs UAE, we offer the CNGB3 Gene Achromatopsia type 3 Genetic Test to help diagnose and provide important information for genetic counseling and treatment planning.

Test Components

The CNGB3 Gene Achromatopsia type 3 Genetic Test includes the following components:

  • NGS Technology
  • Ophthalmology Disorders
  • Genetics

Price

The cost of the CNGB3 Gene Achromatopsia type 3 Genetic Test is 4400.0 AED.

Sample Condition

We accept the following sample conditions for the test:

  • Blood
  • Extracted DNA
  • One drop Blood on FTA Card

Report Delivery

The report will be delivered within 3 to 4 weeks.

Method

The test utilizes NGS (Next-Generation Sequencing) technology.

Test Type

The CNGB3 Gene Achromatopsia type 3 Genetic Test falls under the category of Ophthalmology Disorders.

Doctor

The test is conducted by an Ophthalmologist.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is going for the CNGB3 Gene Achromatopsia type 3 NGS Genetic DNA Test. A Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with the CNGB3 Gene Achromatopsia type 3 NGS Genetic DNA Test gene CNGB3.

Test Details

The CNGB3 gene is associated with a rare genetic condition called Achromatopsia type 3. This condition causes color blindness, poor visual acuity, and extreme sensitivity to light. The CNGB3 Gene Achromatopsia type 3 NGS Genetic Test uses NGS technology to analyze the CNGB3 gene for mutations and variants that may cause Achromatopsia type 3. This test is crucial for diagnosing the condition and providing important information for genetic counseling and treatment planning.

Test Name CNGB3 Gene Achromatopsia type 3 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 CNGB3 Gene Achromatopsia type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CNGB3 Gene Achromatopsia type 3 NGS Genetic DNA Test gene CNGB3
Test Details

The CNGB3 gene is associated with a rare genetic condition called Achromatopsia type 3, which causes color blindness, poor visual acuity, and extreme sensitivity to light.

NGS (Next-Generation Sequencing) Genetic Test is a high-throughput DNA sequencing technology that enables the identification of genetic variations in an individual’s DNA.

The CNGB3 Gene Achromatopsia type 3 NGS Genetic Test is a diagnostic test that uses NGS technology to analyze the CNGB3 gene for mutations and variants that may cause Achromatopsia type 3. This test can help diagnose the condition and provide important information for genetic counseling and treatment planning.