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GGCX Gene Vitamin K-Dependent Clotting Factors Combined Deficiency Type 1 Genetic Test Cost

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

-21%

The GGCX Gene Vitamin K-Dependent Clotting Factors Combined Deficiency Type 1 Genetic Test is a specialized diagnostic assessment available at DNA Labs UAE, designed to identify mutations in the GGCX gene. These mutations can lead to a rare disorder known as Combined Deficiency of Vitamin K-Dependent Clotting Factors Type 1, which affects the body’s ability to properly utilize vitamin K for blood clotting. This condition can result in a range of bleeding issues, from mild to severe.

The test, priced at 4400 AED, involves collecting a DNA sample from the patient, typically through a blood draw or a cheek swab. The sample is then analyzed in the laboratory to detect any genetic anomalies in the GGCX gene that might impair the function of vitamin K-dependent proteins necessary for blood coagulation.

Identifying these genetic mutations can be crucial for the management and treatment of affected individuals, allowing for personalized treatment plans that can include vitamin K supplementation and other supportive therapies. The test is a vital tool for families with a history of bleeding disorders or for individuals showing symptoms related to vitamin K-dependent clotting factor deficiencies. Through early detection and intervention, patients can achieve a better quality of life and reduce the risk of serious bleeding complications.

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GGCX Gene Vitamin K-dependent clotting factors combined deficiency type 1 Genetic Test

Welcome to DNA Labs UAE, where we offer the GGCX Gene Vitamin K-dependent clotting factors combined deficiency type 1 Genetic Test. This test is designed to analyze the GGCX gene and provide valuable information about the presence or absence of mutations associated with vitamin K-dependent clotting factors combined deficiency type 1.

Test Components

The GGCX Gene Vitamin K-dependent clotting factors combined deficiency type 1 Genetic Test includes the following 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: Hematology
  • Doctor: Hematologist
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the GGCX Gene Vitamin K-dependent clotting factors combined deficiency type 1 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 GGCX Gene Vitamin K-dependent clotting factors combined deficiency type 1.

Test Details

The GGCX gene is responsible for producing an enzyme called gamma-glutamyl carboxylase, which plays a role in the activation of vitamin K-dependent clotting factors in the blood. Mutations in the GGCX gene can result in a condition known as vitamin K-dependent clotting factors combined deficiency type 1.

NGS (Next-Generation Sequencing) genetic testing is used to analyze the DNA sequence of the GGCX gene. This testing method can identify specific mutations or variations in the GGCX gene associated with vitamin K-dependent clotting factors combined deficiency type 1. By analyzing the DNA sequence, NGS genetic testing can aid in the diagnosis and understanding of the genetic basis of this condition.

Healthcare providers can utilize this information to determine appropriate treatment options and provide genetic counseling for affected individuals and their families.

For more information or to schedule an appointment for the GGCX Gene Vitamin K-dependent clotting factors combined deficiency type 1 Genetic Test, please contact DNA Labs UAE.

Test Name GGCX Gene Vitamin K-dependent clotting factors combined deficiency type 1 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 Hematology
Doctor Hematologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for GGCX Gene Vitamin K-dependent clotting factors combined deficiency type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GGCX Gene Vitamin K-dependent clotting factors combined deficiency type 1 NGS Genetic DNA Test gene GGCX
Test Details

The GGCX gene is responsible for producing an enzyme called gamma-glutamyl carboxylase, which is involved in the activation of vitamin K-dependent clotting factors in the blood. Mutations in the GGCX gene can lead to a condition known as vitamin K-dependent clotting factors combined deficiency type 1.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of a particular gene or a set of genes. In the context of GGCX gene mutations, NGS genetic testing can be used to identify specific mutations or variations in the GGCX gene that may be associated with vitamin K-dependent clotting factors combined deficiency type 1.

By analyzing the DNA sequence, NGS genetic testing can provide valuable information about the presence or absence of mutations in the GGCX gene, which can help in diagnosing and understanding the genetic basis of vitamin K-dependent clotting factors combined deficiency type 1. This information can be useful for healthcare providers in determining appropriate treatment options and genetic counseling for affected individuals and their families.

SKU: TEST-3968 Category:

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