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ZFHX4 Gene Ptosis Congenital Genetic Test

4,400 د.إ

-21%

The ZFHX4 gene is implicated in a variety of genetic conditions, including congenital ptosis, a condition characterized by the drooping of the upper eyelid present at birth. This condition can affect one or both eyes and varies in severity. It can be purely cosmetic or significantly impair vision depending on the extent of the eyelid droop. The ZFHX4 gene plays a critical role in the development and function of muscles and nerves associated with eyelid movement.

To diagnose and understand the genetic basis of congenital ptosis, DNA Labs UAE offers a specialized genetic test targeting the ZFHX4 gene. This test is designed to identify mutations or alterations in the ZFHX4 gene that may contribute to the development of congenital ptosis. Understanding the genetic underpinnings of this condition can aid in prognosis, management, and treatment planning. It can also provide valuable information for genetic counseling, especially for families with a history of this condition.

The test cost is set at 4400 AED, reflecting the specialized nature of the genetic analysis and the comprehensive service provided by DNA Labs UAE. This includes the collection of a DNA sample, typically through a blood draw or cheek swab, the genetic sequencing or analysis to identify any mutations in the ZFHX4 gene, and a detailed report of the findings. The report may also offer guidance on potential treatment options and recommendations for further genetic counseling if necessary.

By opting for this genetic test, patients and their families can gain insight into the genetic basis of congenital ptosis, enabling informed decisions about their healthcare and future family planning.

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ZFHX4 Gene Ptosis Congenital Genetic Test

At DNA Labs UAE, we offer the ZFHX4 gene Ptosis congenital genetic test to help diagnose and understand this condition. Ptosis refers to the drooping of the upper eyelid, which can partially or completely cover the eye. It is present from birth and can affect one or both eyes.

Test Details

The ZFHX4 gene is associated with Ptosis congenital. To identify any variations or mutations in the ZFHX4 gene that may be causing the condition, we use Next-Generation Sequencing (NGS) technology. NGS genetic testing allows us to analyze multiple genes simultaneously, providing a comprehensive evaluation of genetic variants associated with Ptosis congenital.

Test Components

  • Test Name: ZFHX4 Gene Ptosis congenital 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: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the ZFHX4 gene Ptosis congenital 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 Ptosis congenital.

Benefits of the Test

The NGS genetic test for ZFHX4 gene Ptosis congenital can be useful in diagnosing individuals with this condition, especially when the cause is not apparent through physical examination alone. It can also help in determining the risk of passing on the condition to future generations and guide appropriate medical management or treatment options.

Consultation and Support

It is important to consult with a healthcare professional or genetic counselor to discuss the benefits, limitations, and potential implications of undergoing NGS genetic testing for ZFHX4 gene Ptosis congenital. They can provide personalized guidance and support throughout the testing process.

Test Name ZFHX4 Gene Ptosis congenital Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for ZFHX4 Gene Ptosis, congenital NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ZFHX4 Gene Ptosis, congenital
Test Details

The ZFHX4 gene is associated with a condition called Ptosis, congenital. Ptosis refers to the drooping of the upper eyelid, which can partially or completely cover the eye. It is present from birth and can affect one or both eyes.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced technology to analyze multiple genes simultaneously. It can provide a comprehensive evaluation of genetic variants associated with a particular condition, such as Ptosis, congenital.

The NGS genetic test for ZFHX4 gene Ptosis, congenital involves sequencing the DNA of an individual to identify any variations or mutations in the ZFHX4 gene that may be causing the condition. By analyzing the genetic information, healthcare professionals can determine the presence of specific genetic variants that are known to be associated with Ptosis, congenital.

This genetic test can be useful in diagnosing individuals with Ptosis, congenital, especially when the cause is not apparent through physical examination alone. It can also help in determining the risk of passing on the condition to future generations and guide appropriate medical management or treatment options.

It is important to consult with a healthcare professional or genetic counselor to discuss the benefits, limitations, and potential implications of undergoing NGS genetic testing for ZFHX4 gene Ptosis, congenital. They can provide personalized guidance and support throughout the testing process.

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