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CEP152 Gene Seckel Syndrome Type 5 Genetic Test Cost

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

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The CEP152 gene plays a crucial role in human genetics, particularly related to Seckel Syndrome Type 5, a rare autosomal recessive disorder characterized by growth retardation, microcephaly, and other congenital anomalies. This condition falls under the broader category of Seckel Syndrome, distinguished by its genetic basis tied to mutations in the CEP152 gene.

DNA Labs UAE offers a specialized genetic test designed to identify mutations in the CEP152 gene, aiding in the diagnosis of Seckel Syndrome Type 5. This test is crucial for families with a history of the condition or those experiencing related symptoms, providing essential information for managing and understanding the disorder. The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately detect and interpret genetic variations associated with this syndrome.

By opting for this genetic test, individuals can gain valuable insights into their genetic makeup, enabling informed decisions regarding health management and family planning. DNA Labs UAE, with its commitment to precision and reliability, ensures that clients receive comprehensive support throughout the testing process, from sample collection to result interpretation.

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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CEP152 Gene Seckel Syndrome Type 5 Genetic Test

At DNA Labs UAE, we offer the CEP152 Gene Seckel syndrome type 5 genetic test for individuals suspected of having this rare genetic disorder. This test can provide important information for diagnosis, genetic counseling, and potential treatment options.

Test Details

The CEP152 gene is associated with Seckel syndrome type 5, a rare genetic disorder characterized by severe growth retardation, microcephaly (small head size), intellectual disability, and other physical abnormalities. Our NGS (Next-Generation Sequencing) technology allows for a comprehensive analysis of the genome, specifically targeting the CEP152 gene.

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 CEP152 Gene Seckel syndrome type 5 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 the condition.

Test Procedure

The CEP152 Gene Seckel syndrome type 5 genetic test involves collecting a DNA sample, typically through a blood or saliva sample. This sample is then subjected to NGS technology, which allows for the identification of mutations or variants in the CEP152 gene.

Results and Benefits

The results of the CEP152 Gene Seckel syndrome type 5 genetic test can provide valuable information for individuals suspected of having this condition. It can help confirm a diagnosis, provide genetic counseling, and potentially guide treatment options.

Conclusion

If you or someone you know is suspected of having Seckel syndrome type 5, our CEP152 Gene Seckel syndrome type 5 genetic test can provide important insights. Contact DNA Labs UAE today to learn more about the test, its cost, and how it can benefit you.

Test Name CEP152 Gene Seckel syndrome type 5 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 CEP152 Gene Seckel syndrome type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CEP152 Gene Seckel syndrome type 5 NGS Genetic DNA Test gene CEP152
Test Details

The CEP152 gene is associated with Seckel syndrome type 5, a rare genetic disorder characterized by severe growth retardation, microcephaly (small head size), intellectual disability, and other physical abnormalities.

NGS (Next-Generation Sequencing) genetic testing refers to a high-throughput sequencing technology that can analyze multiple genes simultaneously. In the case of Seckel syndrome type 5, NGS genetic testing can identify mutations or variants in the CEP152 gene, which can help confirm a diagnosis of the condition.

NGS genetic testing involves collecting a DNA sample, typically through a blood or saliva sample, and then sequencing the DNA to identify any genetic variations or mutations. This technology allows for a more comprehensive analysis of the genome compared to traditional sequencing methods.

The results of the NGS genetic test for the CEP152 gene can provide important information for individuals suspected of having Seckel syndrome type 5. This information can help with diagnosis, genetic counseling, and potentially guide treatment options.

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