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COL4A3 Gene Alport syndrome autosomal recessive Genetic Test Cost

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

-21%

The COL4A3 gene plays a crucial role in the development and function of the kidneys, ears, and eyes. Mutations in this gene are associated with Alport syndrome, a genetic disorder that affects the basement membranes of these organs, leading to progressive kidney disease, hearing loss, and eye abnormalities. The autosomal recessive form of Alport syndrome, which requires both parents to pass on a faulty copy of the COL4A3 gene, is one of the types of this condition.

To diagnose this form of Alport syndrome, a genetic test focusing on the COL4A3 gene is available. This test is crucial for confirming the diagnosis, understanding the inheritance pattern, and making informed decisions about family planning and management of the disease. The test analyzes the DNA to identify mutations in the COL4A3 gene that are known to cause the condition.

In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test. The cost of the test is 4400 AED. Conducting the test at DNA Labs UAE ensures that individuals and families affected by or at risk of Alport syndrome have access to accurate diagnosis and genetic counseling, which are essential for managing the condition effectively. This test is a valuable tool in the early detection and treatment planning for Alport syndrome, ultimately helping to improve the quality of life for those affected.

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COL4A3 Gene Alport Syndrome Autosomal Recessive Genetic Test

Welcome to DNA Labs UAE, where we offer the COL4A3 gene Alport syndrome autosomal recessive genetic test. This test is designed to analyze the COL4A3 gene and diagnose Alport syndrome, an inherited condition that affects the kidneys, ears, and eyes.

Test Components

The COL4A3 gene Alport syndrome autosomal recessive 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: Ear Nose Throat Disorders
  • Doctor: ENT Doctor
  • Test Department: Genetics

Pre-Test Information

Prior to undergoing the COL4A3 gene Alport syndrome autosomal recessive genetic test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by Alport syndrome. This will help in identifying any potential genetic mutations in the COL4A3 gene.

Test Details

The COL4A3 gene is associated with Alport syndrome, a genetic disorder characterized by progressive kidney disease, hearing loss, and eye abnormalities. NGS genetic testing is used to analyze multiple genes simultaneously, including the COL4A3 gene. This test helps identify mutations in both copies of the gene, confirming a diagnosis of Alport syndrome.

Autosomal recessive inheritance means that an individual must inherit two copies of a mutated gene (one from each parent) to develop the disorder. If only one copy of the mutated gene is inherited, the individual is considered a carrier and typically does not exhibit symptoms. Therefore, the autosomal recessive NGS genetic test for the COL4A3 gene is crucial in identifying mutations and providing accurate diagnoses for Alport syndrome.

By offering this genetic test, we aim to provide valuable information for treatment decisions and genetic counseling for affected individuals and their families.

Test Name COL4A3 Gene Alport syndrome autosomal recessive 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 Ear Nose Throat Disorders
Doctor ENT Doctor
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for COL4A3 Gene Alport syndrome, autosomal recessive NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with COL4A3 Gene Alport syndrome, autosomal recessive NGS Genetic DNA Test gene COL4A3
Test Details

The COL4A3 gene is associated with a genetic disorder called Alport syndrome. Alport syndrome is an inherited condition that primarily affects the kidneys, ears, and eyes. It is characterized by progressive kidney disease, hearing loss, and eye abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of Alport syndrome, NGS genetic testing can be used to analyze the COL4A3 gene, along with other genes known to be associated with the condition.

Autosomal recessive inheritance means that an individual must inherit two copies of a mutated gene (one from each parent) in order to develop the disorder. If only one copy of the mutated gene is inherited, the individual is considered a carrier and typically does not exhibit symptoms of the condition.

Therefore, an autosomal recessive NGS genetic test for the COL4A3 gene would be used to identify mutations in both copies of the gene, which would confirm a diagnosis of Alport syndrome. This information can be helpful in guiding treatment decisions and providing genetic counseling to affected individuals and their families.