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EYA1 Gene Branchiootorenal Syndrome Type 1 Genetic Test

4,400 د.إ

-21%

The EYA1 gene test for Branchiootorenal Syndrome Type 1 is a specialized genetic test available at DNA Labs UAE. Priced at 4400 AED, this diagnostic tool is crucial for identifying mutations in the EYA1 gene, which are responsible for the development of Branchiootorenal Syndrome Type 1. This condition is characterized by an array of symptoms including branchial arch anomalies, hearing loss, and renal abnormalities. Early detection through this test can facilitate timely intervention and management of the syndrome. DNA Labs UAE employs state-of-the-art technology to ensure accurate and reliable results, aiding in the better understanding and treatment planning for affected individuals and their families.

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EYA1 Gene Branchiootorenal syndrome type 1 Genetic Test

Introduction

The EYA1 gene is associated with Branchiootorenal syndrome type 1 (BOR1), a genetic disorder characterized by hearing loss and abnormalities of the kidneys, ears, and throat.

Test Details

The EYA1 Gene Branchiootorenal syndrome type 1 Genetic Test is a type of NGS (Next-Generation Sequencing) genetic testing. NGS technology allows for the analysis of multiple genes simultaneously, providing a comprehensive assessment of genetic mutations.

Components and Price

  • Test Name: EYA1 Gene Branchiootorenal syndrome type 1 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

Before undergoing the EYA1 Gene Branchiootorenal syndrome type 1 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 with the EYA1 gene.

Importance of Genetic Testing

NGS genetic testing for BOR1 can provide a definitive diagnosis, which is crucial for guiding treatment and management of the condition. Furthermore, it can offer valuable information for family members who may be at risk of inheriting the disorder.

Genetic Counseling

It is important to note that genetic testing should always be accompanied by genetic counseling. This helps individuals and families understand the implications of the results and make informed decisions about their healthcare.

Conclusion

The EYA1 Gene Branchiootorenal syndrome type 1 Genetic Test offered by DNA Labs UAE is a comprehensive NGS genetic testing method that can provide a definitive diagnosis for BOR1. With a price of 4400.0 AED and a sample condition of blood or extracted DNA, this test can help guide treatment and management decisions while also providing valuable information for at-risk family members.

Test Name EYA1 Gene Branchiootorenal syndrome type 1 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 EYA1 Gene Branchiootorenal syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EYA1 Gene Branchiootorenal syndrome type 1 NGS Genetic DNA Test gene EYA1
Test Details

The EYA1 gene is associated with Branchiootorenal syndrome type 1 (BOR1), which is a genetic disorder characterized by hearing loss and abnormalities of the kidneys, ears, and throat.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that analyzes multiple genes simultaneously using advanced sequencing technology. NGS can detect mutations in the EYA1 gene that may be responsible for BOR1.

NGS genetic testing for BOR1 can provide a definitive diagnosis, which can be important for guiding treatment and management of the condition. It can also provide important information for family members who may be at risk of inheriting the disorder.

It is important to note that genetic testing should always be accompanied by genetic counseling to help individuals and families understand the implications of the results and make informed decisions about their healthcare.