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CRYBB3 Gene Cataract Autosomal Recessive Congenital Nuclear Type 2 Genetic Test

4,400 د.إ

-21%

The “CRYBB3 Gene Cataract Autosomal Recessive Congenital Nuclear Type 2 Genetic Test” is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the CRYBB3 gene that are associated with the development of a specific type of cataract. This condition, known as autosomal recessive congenital nuclear cataract type 2, is characterized by the clouding of the eye’s lens at birth or shortly thereafter, affecting vision. The test is critical for early diagnosis and management of the condition, facilitating personalized treatment plans and potentially preventing severe vision impairment.

The genetic test involves analyzing the patient’s DNA to identify mutations in the CRYBB3 gene, which plays a crucial role in the development and maintenance of lens transparency in the eye. Identifying mutations in this gene can confirm the diagnosis and help in understanding the inheritance pattern within a family, offering insights into the risk for future offspring.

The cost of the test is set at 4400 AED, reflecting the specialized nature of the genetic analysis and the expertise required to interpret the results. Conducted at DNA Labs UAE, a facility known for its advanced genetic testing capabilities, this test represents a significant step forward in the early detection and management of congenital cataract conditions, offering hope and improved outcomes for affected individuals and their families.

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CRYBB3 Gene Cataract autosomal recessive congenital nuclear type 2 Genetic Test

At DNA Labs UAE, we offer the CRYBB3 Gene Cataract autosomal recessive congenital nuclear type 2 Genetic Test. This test is designed to diagnose and provide information about the CRYBB3 gene, which is associated with autosomal recessive congenital nuclear cataract type 2.

Test Components

The CRYBB3 Gene Cataract autosomal recessive congenital nuclear type 2 Genetic Test includes the following 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

Prior to the CRYBB3 Gene Cataract autosomal recessive congenital nuclear type 2 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with CRYBB3 Gene Cataract, autosomal recessive congenital nuclear type 2 NGS Genetic DNA Test gene CRYBB3.

Test Details

The CRYBB3 gene is associated with autosomal recessive congenital nuclear cataract type 2. This genetic disorder causes clouding of the lens in the eye from birth. The disorder is caused by mutations in the CRYBB3 gene, which is responsible for producing a protein called beta-crystallin B3. This protein is crucial for the development and maintenance of the lens in the eye.

Our NGS (Next Generation Sequencing) genetic testing method allows for the analysis of multiple genes simultaneously. This test can detect mutations in the CRYBB3 gene and other genes related to cataracts. The process involves taking a small sample of blood or tissue from the patient and analyzing the DNA for mutations.

Early diagnosis of CRYBB3 gene cataract through NGS genetic testing enables appropriate treatment and management. It also provides information about the risk of passing the condition on to future generations. We highly recommend genetic counseling for individuals and families affected by this condition.

Test Name CRYBB3 Gene Cataract autosomal recessive congenital nuclear type 2 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 CRYBB3 Gene Cataract, autosomal recessive congenital nuclear type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CRYBB3 Gene Cataract, autosomal recessive congenital nuclear type 2 NGS Genetic DNA Test gene CRYBB3
Test Details

The CRYBB3 gene is associated with autosomal recessive congenital nuclear cataract type 2. This is a genetic disorder that causes clouding of the lens in the eye from birth. The disorder is caused by mutations in the CRYBB3 gene, which provides instructions for making a protein called beta-crystallin B3. This protein is essential for the development and maintenance of the lens in the eye.

NGS (Next Generation Sequencing) genetic testing is a type of DNA sequencing that allows for the analysis of multiple genes at once. This test can detect mutations in the CRYBB3 gene and other genes associated with cataracts. The test involves taking a small sample of blood or tissue from the patient and analyzing the DNA for mutations.

NGS genetic testing for CRYBB3 gene cataract can help diagnose the condition early, allowing for appropriate treatment and management. It can also provide information about the risk of passing the condition on to future generations. Genetic counseling is recommended for individuals and families affected by this condition.