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. |
