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TCF12 Gene Craniosynostosis Type 3 Genetic Test Cost

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

-21%

The TCF12 gene craniosynostosis type 3 genetic test is a specialized diagnostic procedure aimed at identifying mutations in the TCF12 gene, which are known to cause craniosynostosis type 3. Craniosynostosis is a congenital condition characterized by the premature fusion of one or more of the skull’s sutures, leading to an abnormal head shape and, potentially, developmental issues due to restricted brain growth. The TCF12 gene plays a critical role in the development of the skull, and mutations in this gene can disrupt normal suture formation.

This genetic test is crucial for early diagnosis and management of the condition, enabling healthcare providers to offer appropriate treatment options and interventions to mitigate the effects of premature suture closure. Early intervention can significantly improve outcomes for affected individuals.

The test is conducted at DNA Labs UAE, a leading facility known for its advanced genetic testing services. The cost of the TCF12 gene craniosynostosis type 3 genetic test is 4400 AED. DNA Labs UAE utilizes cutting-edge technology to ensure accurate and reliable results, providing essential information for the effective management of craniosynostosis type 3. This test is an invaluable tool for families seeking answers and options in the face of this challenging condition.

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  • This test is not intended for medical diagnosis or treatment
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TCF12 Gene Craniosynostosis Type 3 Genetic Test

Are you concerned about craniosynostosis type 3 in your family? DNA Labs UAE offers the TCF12 Gene Craniosynostosis Type 3 Genetic Test to help diagnose this condition accurately. Read on to learn more about the test, its components, cost, symptoms, diagnosis, and more.

Test Name: TCF12 Gene Craniosynostosis Type 3 Genetic Test

  • Components: NGS Technology
  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Test Type: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the TCF12 Gene Craniosynostosis Type 3 Genetic Test, it is essential 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 TCF12 Gene Craniosynostosis Type 3 NGS Genetic DNA Test gene TCF12.

Test Details

The TCF12 gene is associated with craniosynostosis type 3, a condition characterized by the premature fusion of skull bones in infants. This fusion can result in an abnormal skull shape and potentially hinder brain growth. NGS (Next-Generation Sequencing) genetic testing is employed to analyze an individual’s DNA for specific genetic variations or mutations. In the case of craniosynostosis type 3, NGS genetic testing can identify mutations or variations in the TCF12 gene that may be causing the condition. By identifying these genetic variations, healthcare professionals can provide a more accurate diagnosis, assess the risk of craniosynostosis in family members, and guide treatment decisions.

It is crucial to note that genetic testing should always be conducted under the guidance of a healthcare professional or genetic counselor. These professionals can help interpret the test results and provide appropriate counseling and support.

If you suspect craniosynostosis type 3 in your family, don’t hesitate to reach out to DNA Labs UAE for the TCF12 Gene Craniosynostosis Type 3 Genetic Test. Early detection and diagnosis can make a significant difference in managing this condition effectively.

Test Name TCF12 Gene Craniosynostosis type 3 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 TCF12 Gene Craniosynostosis type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TCF12 Gene Craniosynostosis type 3 NGS Genetic DNA Test gene TCF12
Test Details

The TCF12 gene is associated with craniosynostosis type 3, which is a condition characterized by the premature fusion of the skull bones in infants. This can lead to abnormal skull shape and potentially restrict brain growth.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze an individual’s DNA for specific genetic variations or mutations. In the case of craniosynostosis type 3, NGS genetic testing can be used to identify mutations or variations in the TCF12 gene that may be causing the condition.

By identifying these genetic variations, healthcare professionals can provide a more accurate diagnosis, assess the risk of craniosynostosis in family members, and potentially guide treatment decisions.

It is important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor, who can help interpret the results and provide appropriate counseling and support.

SKU: TEST-4079 Category:

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