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FYCO1 Gene Cataract Autosomal Recessive Congenital Type 2 Genetic Test

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

-21%

The “FYCO1 Gene Cataract Autosomal Recessive Congenital Type 2 Genetic Test” is a specialized diagnostic examination designed to detect mutations in the FYCO1 gene, which are linked to the development of Autosomal Recessive Congenital Cataracts Type 2 (ARCC2). This condition is a rare, hereditary eye disorder that manifests from birth or early childhood, leading to clouding of the lens in the eye and potentially severe visual impairment or blindness if not diagnosed and managed appropriately.

The test is crucial for families with a history of this condition, as it aids in early detection, allowing for timely intervention and management strategies to preserve vision. It involves analyzing the patient’s DNA to identify mutations in the FYCO1 gene, which plays a significant role in lens development and clarity. By pinpointing these genetic alterations, healthcare providers can confirm a diagnosis of ARCC2, guide treatment decisions, and offer genetic counseling to affected families.

Offered by DNA Labs UAE, the test cost is 4400 AED. DNA Labs UAE is equipped with advanced genetic testing facilities and expertise, ensuring high accuracy and reliability of the test results. This test is an important tool in the field of genetic ophthalmology, offering hope and crucial information for individuals and families grappling with the challenges of congenital cataracts.

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FYCO1 Gene Cataract Autosomal Recessive Congenital Type 2 Genetic Test

Components:

  • Test Name: FYCO1 Gene Cataract Autosomal Recessive Congenital Type 2 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: Clinical History of Patient who is going for FYCO1 Gene Cataract, autosomal recessive congenital type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FYCO1 Gene Cataract, autosomal recessive congenital type 2 NGS Genetic DNA Test gene FYCO1

Test Details:

The FYCO1 gene is associated with the autosomal recessive congenital cataract type 2. This type of cataract is present at birth or develops during infancy and is caused by mutations in the FYCO1 gene. The FYCO1 gene provides instructions for making a protein that is involved in the process of autophagy, which is the body’s way of breaking down and recycling damaged or unnecessary cellular components. Mutations in the FYCO1 gene can disrupt this process and lead to the accumulation of damaged proteins in the lens of the eye, which can cause cataracts.

NGS genetic testing is a type of genetic testing that uses next-generation sequencing technology to analyze multiple genes simultaneously. This type of testing can be used to identify mutations in the FYCO1 gene that are associated with congenital cataract type 2. NGS genetic testing can help diagnose this condition and provide information about the inheritance pattern, which can be useful for family planning and genetic counseling.

Test Name FYCO1 Gene Cataract autosomal recessive congenital 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 FYCO1 Gene Cataract, autosomal recessive congenital type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FYCO1 Gene Cataract, autosomal recessive congenital type 2 NGS Genetic DNA Test gene FYCO1
Test Details

The FYCO1 gene is associated with the autosomal recessive congenital cataract type 2. This type of cataract is present at birth or develops during infancy and is caused by mutations in the FYCO1 gene. The FYCO1 gene provides instructions for making a protein that is involved in the process of autophagy, which is the body’s way of breaking down and recycling damaged or unnecessary cellular components. Mutations in the FYCO1 gene can disrupt this process and lead to the accumulation of damaged proteins in the lens of the eye, which can cause cataracts.

NGS genetic testing is a type of genetic testing that uses next-generation sequencing technology to analyze multiple genes simultaneously. This type of testing can be used to identify mutations in the FYCO1 gene that are associated with congenital cataract type 2. NGS genetic testing can help diagnose this condition and provide information about the inheritance pattern, which can be useful for family planning and genetic counseling.

SKU: TEST-936 Category:

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