Sale!

KRT6B Gene Pachyonychia Congenita Type 4 Genetic Test Cost

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

-21%

The KRT6B Gene Pachyonychia Congenita Type 4 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the KRT6B gene, which are responsible for Pachyonychia Congenita Type 4. This rare genetic disorder is characterized by thickened nails, painful palmoplantar keratoderma, cysts, and other skin abnormalities. The test is crucial for accurate diagnosis, allowing for appropriate management and genetic counseling. At a cost of 4400 AED, this test offers individuals and families critical insights into the genetic basis of the condition, facilitating informed healthcare decisions.

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

KRT6B Gene Pachyonychia congenita type 4 Genetic Test

Welcome to DNA Labs UAE, your trusted genetic testing laboratory. Today, we will be discussing the KRT6B Gene Pachyonychia congenita type 4 Genetic Test. This test is designed to analyze the DNA sequence of the KRT6B gene to identify any mutations or variations associated with Pachyonychia congenita type 4.

Test Details

Pachyonychia congenita type 4 is a rare genetic disorder characterized by thickened nails and other skin abnormalities. Our NGS (Next-Generation Sequencing) genetic testing method allows us to accurately identify mutations or variations in the KRT6B gene that may be present in individuals with this condition.

Components and Price

The cost of the KRT6B Gene Pachyonychia congenita type 4 Genetic Test is AED 4400.0. The test can be performed using either blood or extracted DNA, or by using one drop of blood on an FTA card.

Report Delivery and Method

After the sample is collected, the report will be delivered within 3 to 4 weeks. Our NGS Technology ensures accurate and reliable results for this genetic test.

Test Type and Doctor

The KRT6B Gene Pachyonychia congenita type 4 Genetic Test falls under the categories of Osteology, Dermatology, and Immunology Disorders. The test should be conducted under the supervision of a Dermatologist.

Test Department and Pre Test Information

The KRT6B Gene Pachyonychia congenita type 4 Genetic Test is conducted by our Genetics department. Before undergoing the test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by this genetic disorder.

Conclusion

If you suspect that you or a family member may have Pachyonychia congenita type 4, our KRT6B Gene Pachyonychia congenita type 4 Genetic Test can provide valuable insights. Our qualified healthcare professionals and genetic counselors will interpret the results and provide appropriate guidance and support for managing this condition. Contact DNA Labs UAE today to schedule your genetic test.

Test Name KRT6B Gene Pachyonychia congenita type 4 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for KRT6B Gene Pachyonychia congenita type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KRT6B Gene Pachyonychia congenita type 4 NGS Genetic DNA Test gene KRT6B
Test Details

The KRT6B gene is associated with Pachyonychia congenita type 4, a rare genetic disorder characterized by thickened nails and other skin abnormalities. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of genes to identify mutations or variations that may be associated with a particular condition.

In the context of Pachyonychia congenita type 4, an NGS genetic test would involve sequencing the KRT6B gene to identify any mutations or variations that may be present. This can help in confirming a diagnosis, predicting disease severity, and providing information for genetic counseling and management of the condition.

It is important to note that genetic testing should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.