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HOXD13 Gene Vater Association Genetic Test

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

-21%

The HOXD13 Gene Vater Association Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the HOXD13 gene, which are associated with VACTERL association. VACTERL association is a rare condition characterized by the non-random co-occurrence of vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities. The test plays a crucial role in the early detection and management of these conditions, offering insights that can guide clinical decisions and personalized care plans.

Conducted in the advanced facilities of DNA Labs UAE, this genetic test requires a sample of the patient’s DNA, usually obtained through a blood draw. The process involves analyzing the specific sequences of the HOXD13 gene to identify any mutations that might predispose individuals to the components of VACTERL association.

The cost of the HOXD13 Gene Vater Association Genetic Test at DNA Labs UAE is set at 4400 AED. This price reflects the comprehensive nature of the test, encompassing the sophisticated technology and expertise required to accurately identify and interpret gene mutations. For patients and families facing the possibility of VACTERL association, this test offers valuable genetic insights that can aid in understanding their health risks and in making informed medical and lifestyle 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
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HOXD13 Gene Vater Association Genetic Test

Welcome to DNA Labs UAE, where we offer the HOXD13 Gene Vater Association Genetic Test. This test is designed to identify mutations or variations in the HOXD13 gene that may be associated with a rare genetic disorder called hand-foot-genital syndrome (HFGS).

Test Components

The HOXD13 Gene Vater Association Genetic Test includes:

  • 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

Test Price

The cost of the HOXD13 Gene Vater Association Genetic Test is 4400.0 AED.

Pre Test Information

Prior to undergoing the HOXD13 Gene Vater Association 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 the HOXD13 Gene Vater Association NGS Genetic DNA Test gene HOXD13.

Test Details

The HOXD13 gene is associated with hand-foot-genital syndrome (HFGS), a rare genetic disorder characterized by malformations of the hands, feet, and genitalia. Mutations in the HOXD13 gene can disrupt normal development during embryogenesis, resulting in the characteristic features of HFGS.

Next-Generation Sequencing (NGS) genetic tests are a type of genetic testing that can analyze multiple genes simultaneously. In the case of the HOXD13 gene, an NGS genetic test can identify mutations or variations in the gene that may be associated with HFGS. This type of genetic testing is valuable for diagnosing individuals with HFGS and providing important information for genetic counseling and management of the condition.

Test Name HOXD13 Gene Vater association 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 HOXD13 Gene Vater association NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HOXD13 Gene Vater association NGS Genetic DNA Test gene HOXD13
Test Details

The HOXD13 gene is associated with a rare genetic disorder called hand-foot-genital syndrome (HFGS). HFGS is characterized by malformations of the hands, feet, and genitalia. Mutations in the HOXD13 gene can disrupt normal development during embryogenesis, leading to the characteristic features of HFGS.

NGS (Next-Generation Sequencing) genetic tests are a type of genetic testing that can analyze multiple genes simultaneously. In the context of the HOXD13 gene, an NGS genetic test can be used to identify mutations or variations in the HOXD13 gene that may be associated with HFGS. This type of genetic testing can help diagnose individuals with HFGS and provide valuable information for genetic counseling and management of the condition.

SKU: TEST-4430 Category:

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