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GLI3 Gene Greig Cephalopolysyndactyly Syndrome Genetic Test Cost

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

-21%

The GLI3 Gene Greig Cephalopolysyndactyly Syndrome Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the GLI3 gene that are associated with Greig cephalopolysyndactyly syndrome (GCPS). GCPS is a rare genetic disorder characterized by physical abnormalities, including an unusually large head size (macrocephaly), widely spaced eyes (ocular hypertelorism), and a combination of polydactyly (extra fingers or toes) and syndactyly (fusion of fingers or toes). These features can vary significantly in severity among affected individuals.

The test is conducted through a blood sample or cheek swab, which is then analyzed for specific genetic alterations in the GLI3 gene that are known to cause the syndrome. This genetic test is critical for accurate diagnosis, allowing for appropriate management and treatment plans, as well as genetic counseling for families.

Priced at 4400 AED, the GLI3 Gene Greig Cephalopolysyndactyly Syndrome Genetic Test at DNA Labs UAE is a valuable resource for individuals and families seeking clarity on this genetic condition, providing them with essential information for making informed health 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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GLI3 Gene Greig Cephalopolysyndactyly Syndrome Genetic Test

At DNA Labs UAE, we offer the GLI3 Gene Greig Cephalopolysyndactyly Syndrome Genetic Test at a cost of AED 4400.0.

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

Before undergoing the GLI3 Gene Greig Cephalopolysyndactyly 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 GLI3 Gene Greig Cephalopolysyndactyly Syndrome NGS Genetic DNA Test gene GLI3.

Test Details

The GLI3 gene is associated with Greig cephalopolysyndactyly syndrome (GCPS), a rare genetic disorder characterized by craniofacial abnormalities and limb malformations. NGS (Next-Generation Sequencing) genetic testing is utilized to analyze the GLI3 gene and identify any mutations or variants that may be present. NGS is a high-throughput sequencing technology that allows for the simultaneous sequencing of multiple genes or even the entire genome.

In the case of GCPS, NGS can be used to sequence the GLI3 gene and identify any variations in the DNA sequence that may be associated with the disorder. By analyzing the GLI3 gene using NGS, healthcare professionals can determine if there are any mutations or variants present that may be causing Greig cephalopolysyndactyly syndrome. This information can help with diagnosis, genetic counseling, and potentially guide treatment decisions for individuals with the condition.

Test Name GLI3 Gene Greig cephalopolysyndactyly 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 GLI3 Gene Greig cephalopolysyndactyly syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GLI3 Gene Greig cephalopolysyndactyly syndrome NGS Genetic DNA Test gene GLI3
Test Details

The GLI3 gene is associated with Greig cephalopolysyndactyly syndrome (GCPS), which is a rare genetic disorder characterized by craniofacial abnormalities and limb malformations. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the GLI3 gene and identify any mutations or variants that may be present.

NGS is a high-throughput sequencing technology that allows for the simultaneous sequencing of multiple genes or even the entire genome. In the case of GCPS, NGS can be used to sequence the GLI3 gene and identify any variations in the DNA sequence that may be associated with the disorder.

By analyzing the GLI3 gene using NGS, healthcare professionals can determine if there are any mutations or variants present that may be causing Greig cephalopolysyndactyly syndrome. This information can help with diagnosis, genetic counseling, and potentially guide treatment decisions for individuals with the condition.

SKU: TEST-4126 Category:

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