Nx GEN SEQUENCING: OPHTHALMOPLEGIA Test

Nx GEN SEQUENCING: OPHTHALMOPLEGIA Test

Disease: Weakness of Eye muscles

Method: NGS, Sanger sequencing

DNA Labs India is Ranked as No1 genetic DNA Test lab- 3500 Sample collection centers across India Call 07941057551 to talk with Doctor to get second opinion for free of cost - 100% All Conversation are private and confidential

Call 07941057551 Dr Vijaya

Sample Types
  • 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.

28,665.00/- Rs ₹31,850.0010% off

  • Results in : Sample Daily by 9 am; Report 45 Working days

Why to get tested at DNA Labs India for Nx GEN SEQUENCING: OPHTHALMOPLEGIA Test ?

Book Now
  • 3500 Sample collection centers, Free Home Sample collection for Nx GEN SEQUENCING: OPHTHALMOPLEGIA Test in your city
  • Ranked India No1 DNA Test Lab for Nx GEN SEQUENCING: OPHTHALMOPLEGIA Test
  • Most Trusted Lab by doctors for Nx GEN SEQUENCING: OPHTHALMOPLEGIA Test. Call 07941057551 to talk with Doctor to get second opinion for free of cost
  • 100% All Conversation are private and confidential Call 07941057551 to talk with doctor 100% Accurate Test Results for Nx GEN SEQUENCING: OPHTHALMOPLEGIA Test

Nx GEN SEQUENCING: OPHTHALMOPLEGIA Test Cost 28665 Rs


Test Name Nx GEN SEQUENCING: OPHTHALMOPLEGIA Test
Test type Ophthalmologist
Pre-test Information Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.
Report Delivery Sample Daily by 9 am; Report 45 Working days
Components C10orf2, DNA2, OPA1, POLG, POLG2, RRM2B, SLC25A4, TYMP
Price ₹ 28665
Method NGS, Sanger sequencing

Nx GEN SEQUENCING: OPHTHALMOPLEGIA Test Details


Short Description

Ophthalmoplegia is a progressive condition characterized by weakness of the eye muscles. It typically appears in adults between 18 to 40 years of age and slowly worsens over time. Mutations in several different genes on different chromosomes are associated with Ophthalmoplegia. This test is useful for the genetic determination of this disorder.

Test Specifications

  • Speciality: Ophthalmologist

  • Components: C10orf2, DNA2, OPA1, POLG, POLG2, RRM2B, SLC25A4, TYMP

  • Department: MOLECULAR DIAGNOSTICS

  • Shipping Stability: Room Temperature: 6 hrs, Refrigerator:72 hrs, Frozen: NA

PreTest Information

Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.

Detail Description

Nx GEN SEQUENCING: OPHTHALMOPLEGIA Test cost INR:28665 symptoms diagnosis

Are you or someone you know experiencing symptoms of ophthalmoplegia? This condition is characterized by weakness or paralysis of the eye muscles, which can lead to double vision, drooping eyelids, and difficulty moving the eyes. There are many potential causes of ophthalmoplegia, including nerve damage, muscle disorders, and brain injuries. One potential tool for diagnosing the underlying cause of ophthalmoplegia is Nx GEN SEQUENCING.

What is Nx GEN SEQUENCING?

Nx GEN SEQUENCING is a type of genetic testing that can help identify mutations in a person's DNA that may be contributing to their symptoms. This test uses advanced sequencing technology to analyze a person's entire genome, looking for changes or abnormalities that could be causing their condition.

How can Nx GEN SEQUENCING help diagnose ophthalmoplegia?

For people with ophthalmoplegia, Nx GEN SEQUENCING can help identify any genetic mutations that may be contributing to their symptoms. This can be particularly helpful in cases where other diagnostic tests have not provided a clear answer. By identifying the specific genetic mutations that are causing ophthalmoplegia, doctors can develop more targeted treatment plans and better manage a patient's symptoms.

What are the symptoms of ophthalmoplegia?

The symptoms of ophthalmoplegia can vary depending on the underlying cause of the condition. However, some common symptoms include:

  • Double vision
  • Drooping eyelids
  • Difficulty moving the eyes
  • Eye pain
  • Headaches
  • Nausea and vomiting

How is ophthalmoplegia diagnosed?

Diagnosing ophthalmoplegia typically involves a thorough medical history and physical exam, as well as a variety of diagnostic tests. These may include:

  • Eye movement tests
  • Muscle strength tests
  • Blood tests
  • Imaging tests, such as MRI or CT scans

If these tests do not provide a clear answer, Nx GEN SEQUENCING may be recommended to help identify any genetic mutations that may be contributing to the condition.

What is the cost of Nx GEN SEQUENCING for ophthalmoplegia?

The cost of Nx GEN SEQUENCING for ophthalmoplegia can vary depending on the specific test and the laboratory conducting the test. At DNA Labs India, the cost of the test is INR 28,665. This includes the cost of the test itself, as well as any consultation or support services that may be needed.

Conclusion

If you or someone you know is experiencing symptoms of ophthalmoplegia, it is important to seek medical attention and receive a proper diagnosis. Nx GEN SEQUENCING can be a valuable tool in helping to identify the genetic mutations that may be contributing to the condition, allowing for more targeted treatment and management of symptoms. At DNA Labs India, we offer a range of genetic testing services, including Nx GEN SEQUENCING for ophthalmoplegia. Contact us today to learn more.

Ophthalmoplegia is a progressive condition characterized by weakness of the eye muscles. It typically appears in adults between 18 to 40 years of age and slowly worsens over time. Mutations in several different genes on different chromosomes are associated with Ophthalmoplegia. This test is useful for the genetic determination of this disorder.

Frequently Asked Questions

  • What is the cost of Nx GEN SEQUENCING: OPHTHALMOPLEGIA Test?

    Cost of Nx GEN SEQUENCING: OPHTHALMOPLEGIA Test is 28665 Rs

₹28,665.00 ₹31,850.0010% off

Book Now
  • Free Home Sample collection
  • Ranked India No1 DNA Test Lab
  • Most Trusted Lab by doctors
  • 100% Accurate Test Results