EYA4 Gene Deafness Autosomal Dominant Type 10 Genetic Test
Are you or your loved ones experiencing hearing loss? DNA Labs UAE offers the EYA4 Gene Deafness Autosomal Dominant Type 10 Genetic Test, a comprehensive genetic test that can help diagnose and provide valuable information for genetic counseling and family planning.
Test Components and Price
The EYA4 Gene Deafness Autosomal Dominant Type 10 Genetic Test is priced at AED 4400.0. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.
Report Delivery and Method
After sample collection, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology, which allows for the simultaneous analysis of multiple genes.
Test Type and Doctor
The EYA4 Gene Deafness Autosomal Dominant Type 10 Genetic Test falls under the category of Ear Nose Throat Disorders. It is recommended to consult with an ENT Doctor for this test.
Test Department and Pre Test Information
This genetic test is conducted in the Genetics department. Prior to the test, it is important to provide the clinical history of the patient who is undergoing the SLC52A3 Gene Brown-Vialetto-Van Laere Syndrome 1 NGS Genetic DNA Test. A Genetic Counseling session will be conducted to draw a pedigree chart of family members affected by the SLC52A3 Gene Brown-Vialetto-Van Laere Syndrome 1 NGS Genetic DNA Test gene SLC52A4.
Understanding the EYA4 Gene Deafness Autosomal Dominant Type 10 Genetic Test
The EYA4 gene is associated with a type of deafness called autosomal dominant type 10 (DFNA10). In autosomal dominant conditions, a single copy of the mutated gene is sufficient to cause the condition. The NGS genetic test for EYA4 gene deafness involves sequencing the EYA4 gene to identify any mutations or variations that may be responsible for the hearing loss.
This genetic test is essential in diagnosing individuals with DFNA10, determining the inheritance pattern within families, and providing information for genetic counseling and family planning.
It is crucial to note that genetic testing should always be performed by a qualified healthcare professional or genetic counselor. They can interpret the results accurately and provide appropriate guidance and support based on the findings.
| Test Name | EYA4 Gene Deafness autosomal dominant type 10 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 SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test gene SLC52A4 |
| Test Details |
The EYA4 gene is associated with a type of deafness known as autosomal dominant type 10 (DFNA10). Autosomal dominant means that a single copy of the mutated gene is sufficient to cause the condition. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the case of EYA4 gene deafness, an NGS genetic test would involve sequencing the EYA4 gene to identify any mutations or variations that may be responsible for the hearing loss. This type of genetic testing can help diagnose individuals with DFNA10, determine the inheritance pattern within families, and provide information for genetic counseling and family planning. It’s important to note that genetic testing should be performed by a qualified healthcare professional or genetic counselor, who can interpret the results and provide appropriate guidance and support. |
