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EVC2 Gene Ellis-van Creveld Syndrome Genetic Test Cost

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

-21%

The EVC2 Gene Ellis-van Creveld Syndrome Genetic Test is a specialized diagnostic examination available at DNA Labs UAE, designed to detect mutations in the EVC2 gene, which are associated with Ellis-van Creveld Syndrome (EVC). EVC is a rare genetic disorder characterized by short stature, polydactyly, nail dysplasia, dental abnormalities, and congenital heart defects. The test plays a crucial role in the early diagnosis and management of the syndrome, allowing for timely intervention and counseling for affected individuals and their families. Priced at 4400 AED, the test involves analyzing the patient’s DNA to identify specific genetic alterations in the EVC2 gene, providing a reliable diagnosis of Ellis-van Creveld Syndrome. Conducted at DNA Labs UAE, the test adheres to high standards of accuracy and confidentiality, ensuring patients receive comprehensive support and information regarding their genetic health.

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EVC2 Gene Ellis-van Creveld syndrome Genetic Test

At DNA Labs UAE, we offer the EVC2 Gene Ellis-van Creveld syndrome Genetic Test at a cost of AED 4400.0. This test helps in diagnosing and identifying mutations or variants in the EVC2 gene associated with Ellis-van Creveld syndrome.

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

Prior to undergoing the EVC2 Gene Ellis-van Creveld syndrome NGS Genetic DNA 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 the EVC2 gene. This information will aid in the analysis and interpretation of the test results.

Test Details

The EVC2 gene is responsible for Ellis-van Creveld syndrome, a rare genetic disorder characterized by short stature, skeletal abnormalities, heart defects, and extra fingers or toes. Our NGS genetic testing utilizes Next-Generation Sequencing technology to analyze the EVC2 gene and identify any mutations or variants present. This approach allows for the simultaneous analysis of multiple genes, making it a more efficient and comprehensive method compared to traditional sequencing.

The EVC2 Gene Ellis-van Creveld syndrome Genetic Test is not only useful in confirming a diagnosis of Ellis-van Creveld syndrome but also provides valuable information for genetic counseling and management of the condition. Additionally, it can be used for carrier testing in individuals with a family history of the disorder.

Before undergoing this test, it is highly recommended to consult with a genetic counselor or healthcare provider to discuss the benefits, limitations, and implications of genetic testing for Ellis-van Creveld syndrome. They will provide guidance and support throughout the testing process.

Test Name EVC2 Gene Ellis-van Creveld 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 EVC2 Gene Ellis-van Creveld syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EVC2 Gene Ellis-van Creveld syndrome NGS Genetic DNA Test gene EVC2
Test Details

The EVC2 gene is associated with Ellis-van Creveld syndrome, which is a rare genetic disorder characterized by short stature, skeletal abnormalities, and various other features such as heart defects and extra fingers or toes.

NGS (Next-Generation Sequencing) genetic testing can be used to analyze the EVC2 gene and identify any mutations or variants that may be present. This type of testing allows for the simultaneous analysis of multiple genes, making it a more efficient and comprehensive approach compared to traditional sequencing methods.

By identifying mutations in the EVC2 gene, NGS testing can help confirm a diagnosis of Ellis-van Creveld syndrome and provide valuable information for genetic counseling and management of the condition. It can also be used for carrier testing in individuals with a family history of the disorder.

It is important to consult with a genetic counselor or healthcare provider to discuss the benefits, limitations, and implications of genetic testing for Ellis-van Creveld syndrome before undergoing the test.

SKU: TEST-4103 Category:

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