FOXI1 Gene Deafness Autosomal Recessive Type 4 Genetic Test
Welcome to DNA Labs UAE, a leading genetic lab offering a wide range of genetic tests. In this blog post, we will be discussing the FOXI1 Gene Deafness Autosomal Recessive Type 4 Genetic Test. Read on to learn more about this test, including its cost, symptoms, diagnosis, and more.
Test Name: FOXI1 Gene Deafness Autosomal Recessive Type 4 Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
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 SLC52A11
Test Details
The FOXI1 gene is associated with a type of deafness known as autosomal recessive type 4 deafness. Autosomal recessive inheritance means that an individual must inherit two copies of the mutated gene (one from each parent) in order to develop the condition.
NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It can identify mutations or variations in specific genes, such as the FOXI1 gene, that may be associated with certain genetic conditions or traits.
In the context of FOXI1 gene deafness, an NGS genetic test would involve sequencing the FOXI1 gene to identify any mutations or variations that may be causing or contributing to the individual’s deafness. This information can help with diagnosis, prognosis, and potentially guide treatment options or genetic counseling for affected individuals and their families.
Thank you for reading our blog post on the FOXI1 Gene Deafness Autosomal Recessive Type 4 Genetic Test. If you have any further questions or would like to schedule a test, please contact DNA Labs UAE.
| Test Name | FOXI1 Gene Deafness autosomal recessive type 4 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 SLC52A11 |
| Test Details |
The FOXI1 gene is associated with a type of deafness known as autosomal recessive type 4 deafness. Autosomal recessive inheritance means that an individual must inherit two copies of the mutated gene (one from each parent) in order to develop the condition. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It can identify mutations or variations in specific genes, such as the FOXI1 gene, that may be associated with certain genetic conditions or traits. In the context of FOXI1 gene deafness, an NGS genetic test would involve sequencing the FOXI1 gene to identify any mutations or variations that may be causing or contributing to the individual’s deafness. This information can help with diagnosis, prognosis, and potentially guide treatment options or genetic counseling for affected individuals and their families. |
