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Nx GEN Sequencing Usher Syndrome Test

5,730 د.إ

-10%

The Nx Gen Sequencing Usher Syndrome Test is a cutting-edge diagnostic tool available at DNA Labs UAE, designed to accurately identify genetic markers associated with Usher Syndrome. Usher Syndrome is a rare genetic disorder that leads to a combination of hearing loss and visual impairment, significantly affecting the quality of life. This test utilizes next-generation sequencing technology to analyze the patient’s DNA, targeting specific genes known to be linked with the syndrome, providing a comprehensive understanding of the genetic mutations present.

At a cost of 5730 AED, the test is conducted in the state-of-the-art facilities of DNA Labs UAE, ensuring high precision and reliability. It is particularly valuable for individuals with a family history of Usher Syndrome or those exhibiting symptoms, offering crucial insights for early intervention and management strategies. By opting for this advanced genetic test, patients and healthcare providers can make informed decisions regarding future healthcare plans, potentially mitigating the progression of symptoms associated with Usher Syndrome.

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  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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Nx GEN SEQUENCING USHER SYNDROME Test

Test Name: Nx GEN SEQUENCING USHER SYNDROME Test

Components: CDH23, CIB2, CLRN1, DFNB31, ADGRV1, MY- O7A, PCDH15, PDZD7, USH1C, USH1G, USH2A

Price: 5730.0 AED

Sample Condition: Submit 10 mL (5 mL min.) whole blood from 2 Lavender Top (EDTA) tubes. Ship refrigerated. DO NOT FREEZE. Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.

Report Delivery: Sample Daily by 9 am; Report 45 Working days

Method: NGS, Sanger sequencing

Test type: Loss of Hearing & Vision

Doctor: Ophthalmologist, ENT Specialist

Test Department: MOLECULAR DIAGNOSTICS

Pre Test Information: Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.

Test Details

Usher syndrome is a genetic disorder that causes hearing loss and vision impairment. It is a rare condition that affects about 1 in 6,000 to 1 in 10,000 people worldwide. There are three types of Usher syndrome, each with different symptoms and severity.

Nx Gen Sequencing is a genetic testing method that can be used to diagnose Usher syndrome. This test analyzes the DNA of a person to look for mutations in genes that are known to cause the condition. The test can identify mutations in genes such as MYO7A, USH2A, and CDH23, which are commonly associated with Usher syndrome.

The test is performed by collecting a small sample of blood or saliva from the person being tested. The DNA in the sample is then extracted and analyzed using Nx Gen Sequencing technology.

The results of the test can help doctors diagnose Usher syndrome and provide appropriate treatment and support. Early diagnosis of Usher syndrome is important because it allows for early intervention and management of the condition. Treatment may include hearing aids, cochlear implants, and vision aids. In some cases, gene therapy may also be an option.

Overall, Nx Gen Sequencing is a valuable tool for diagnosing Usher syndrome and other genetic disorders. It can provide important information about a person’s health and help them receive appropriate care and support.

Test Name Nx GEN SEQUENCING USHER SYNDROME Test
Components CDH23, CIB2, CLRN1, DFNB31, ADGRV1, MY- O7A, PCDH15, PDZD7, USH1C, USH1G, USH2A
Price 5730.0 AED
Sample Condition Submit 10 mL (5 mL min.) whole blood from 2 Lavender Top (EDTA) tubes. Ship refrigerated. DO NOT FREEZE. Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.
Report Delivery Sample Daily by 9 am; Report 45 Working days
Method NGS, Sanger sequencing
Test type Loss of Hearing & Vision
Doctor Ophthalmologist, ENT Specialist
Test Department: MOLECULAR DIAGNOSTICS
Pre Test Information Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.
Test Details

Usher syndrome is a genetic disorder that causes hearing loss and vision impairment. It is a rare condition that affects about 1 in 6,000 to 1 in 10,000 people worldwide. There are three types of Usher syndrome, each with different symptoms and severity.

Nx Gen Sequencing is a genetic testing method that can be used to diagnose Usher syndrome. This test analyzes the DNA of a person to look for mutations in genes that are known to cause the condition. The test can identify mutations in genes such as MYO7A, USH2A, and CDH23, which are commonly associated with Usher syndrome.

The test is performed by collecting a small sample of blood or saliva from the person being tested. The DNA in the sample is then extracted and analyzed using Nx Gen Sequencing technology. The results of the test can help doctors diagnose Usher syndrome and provide appropriate treatment and support.

Early diagnosis of Usher syndrome is important because it allows for early intervention and management of the condition. Treatment may include hearing aids, cochlear implants, and vision aids. In some cases, gene therapy may also be an option.

Overall, Nx Gen Sequencing is a valuable tool for diagnosing Usher syndrome and other genetic disorders. It can provide important information about a person’s health and help them receive appropriate care and support.