Sale!

MSX1 Gene Witkop Syndrome Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The MSX1 gene plays a crucial role in dental development, and mutations in this gene can lead to Witkop syndrome, also known as tooth-and-nail syndrome. This condition is characterized by nail dysplasia and missing teeth (tooth agenesis). To diagnose this genetic condition, DNA Labs UAE offers a specialized genetic test targeting the MSX1 gene.

The test is designed to identify mutations in the MSX1 gene that are associated with Witkop syndrome. It involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory for genetic abnormalities linked to the syndrome.

The cost of the MSX1 Gene Witkop Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This comprehensive testing not only aids in the diagnosis of Witkop syndrome but also helps in understanding the risk of passing the condition to the next generation, thereby providing essential information for family planning and management of the syndrome.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

MSX1 Gene Witkop Syndrome Genetic Test

At DNA Labs UAE, we offer the MSX1 Gene Witkop Syndrome Genetic Test. This test is designed to analyze the MSX1 gene for any mutations or variants that may be associated with Witkop syndrome, also known as tooth and nail syndrome.

Test Details

Witkop syndrome is a rare genetic disorder characterized by abnormalities in tooth and nail development. Our NGS (Next-Generation Sequencing) technology allows us to analyze multiple genes simultaneously, providing a comprehensive analysis of the MSX1 gene.

Components and Price

The cost of the MSX1 Gene Witkop Syndrome Genetic Test is 4400.0 AED. The test can be conducted using a blood sample, extracted DNA, or one drop of blood on an FTA Card.

Report Delivery

Once the sample is received, the report will be delivered within 3 to 4 weeks.

Method

We use NGS technology for this test, which involves sequencing the DNA obtained from the sample to identify any genetic variations.

Test Type and Doctor

The MSX1 Gene Witkop Syndrome Genetic Test falls under the category of Dysmorphology. It is recommended to consult a pediatrician for this test.

Test Department

This test is conducted in our Genetics department, where our experienced professionals ensure accurate and reliable results.

Pre Test Information

Before undergoing the MSX1 Gene Witkop Syndrome 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 by Witkop syndrome.

Benefits of Genetic Testing for Witkop Syndrome

Genetic testing for Witkop syndrome can be highly beneficial in various ways:

  • Confirmation of diagnosis
  • Identification of the specific genetic cause of the condition
  • Guidance for treatment and management options
  • Information about the risk of having a child with Witkop syndrome for family members

It is important to note that genetic testing for Witkop syndrome, including NGS, should always be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and interpretation of the results.

Test Name MSX1 Gene Witkop syndrome 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for MSX1 Gene Witkop syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MSX1 Gene Witkop syndrome NGS Genetic DNA Test gene MSX1
Test Details

The MSX1 gene is associated with a condition called Witkop syndrome, also known as tooth and nail syndrome. Witkop syndrome is a rare genetic disorder characterized by abnormalities in tooth and nail development.

NGS (Next-Generation Sequencing) is a type of genetic testing that allows for the analysis of multiple genes simultaneously. In the context of Witkop syndrome, NGS can be used to analyze the MSX1 gene for any mutations or variants that may be contributing to the condition.

NGS testing involves obtaining a DNA sample, typically through a blood or saliva sample, and sequencing the DNA to identify any genetic variations. By analyzing the MSX1 gene using NGS, healthcare professionals can determine if there are any mutations or variants present that may be associated with Witkop syndrome.

Genetic testing for Witkop syndrome can be useful in confirming a diagnosis, providing information about the specific genetic cause of the condition, and helping to guide treatment and management options. It can also be beneficial for family members of individuals with Witkop syndrome, as it can provide information about their risk of having a child with the condition.

It is important to note that genetic testing for Witkop syndrome, including NGS, should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and interpretation of the results.