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C12orf57 Gene Temtamy Syndrome Genetic Test

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

-21%

The C12orf57 gene Temtamy syndrome genetic test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the C12orf57 gene, which are associated with Temtamy syndrome. Temtamy syndrome is a rare genetic disorder characterized by a spectrum of developmental anomalies including craniofacial abnormalities, intellectual disability, and other physical malformations. The test plays a crucial role in the early diagnosis and management of the syndrome, allowing for tailored care and intervention strategies.

Priced at 4400 AED, the test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for specific genetic mutations in the C12orf57 gene. The results can provide valuable information for affected individuals and their families regarding the prognosis, potential treatments, and the risk of passing the condition to future generations. Conducted in the state-of-the-art facilities of DNA Labs UAE, this genetic test is a vital tool for clinicians and genetic counselors in the diagnosis and understanding of Temtamy syndrome, ultimately facilitating better patient outcomes.

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C12orf57 Gene Temtamy Syndrome Genetic Test

Welcome to DNA Labs UAE, your trusted genetic lab for all your testing needs. In this blog post, we will be discussing the C12orf57 Gene Temtamy syndrome Genetic Test, its cost, symptoms, diagnosis, and other important details.

Test Name: C12orf57 Gene Temtamy 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:

Before undergoing the C12orf57 Gene Temtamy syndrome NGS Genetic DNA 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 with C12orf57 Gene Temtamy syndrome NGS Genetic DNA Test gene C12orf57.

Test Details:

The C12orf57 gene is associated with a rare genetic disorder called Temtamy syndrome. Next-generation sequencing (NGS) genetic testing is a method used to analyze and identify genetic variations in an individual’s DNA. In the case of Temtamy syndrome, NGS genetic testing can be used to detect any mutations or alterations in the C12orf57 gene that may be causing the disorder.

This test can help confirm a diagnosis, provide information about the specific genetic variant causing the syndrome, and assist in genetic counseling for affected individuals and their families.

By opting for the C12orf57 Gene Temtamy Syndrome Genetic Test at DNA Labs UAE, you can gain valuable insights into this rare genetic disorder and take appropriate steps towards managing and treating it.

For more information or to schedule an appointment, please contact DNA Labs UAE.

Test Name C12orf57 Gene Temtamy 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 C12orf57 Gene Temtamy syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with C12orf57 Gene Temtamy syndrome NGS Genetic DNA Test gene C12orf57
Test Details

The C12orf57 gene is associated with a rare genetic disorder called Temtamy syndrome. Next-generation sequencing (NGS) genetic testing is a method used to analyze and identify genetic variations in an individual’s DNA. In the case of Temtamy syndrome, NGS genetic testing can be used to detect any mutations or alterations in the C12orf57 gene that may be causing the disorder. This test can help confirm a diagnosis, provide information about the specific genetic variant causing the syndrome, and assist in genetic counseling for affected individuals and their families.