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NIN Gene Seckel Syndrome Type 7 Genetic Test Cost

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

-21%

The NIN Gene Seckel Syndrome Type 7 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at detecting mutations in the NIN gene, which are responsible for causing Seckel Syndrome Type 7. This rare genetic disorder is characterized by growth delays, microcephaly (abnormally small head size), and other physical anomalies. The test plays a crucial role in early diagnosis, enabling targeted interventions and management strategies to improve the quality of life for affected individuals. Priced at 4400 AED, the test involves analyzing the patient’s DNA to identify specific genetic alterations in the NIN gene, providing valuable insights for families and healthcare providers. DNA Labs UAE, known for its advanced genetic testing capabilities, ensures accuracy and confidentiality in the testing process, making it a trusted choice for genetic diagnostics in the region.

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NIN Gene Seckel Syndrome Type 7 Genetic Test

At DNA Labs UAE, we offer the NIN Gene Seckel syndrome type 7 Genetic Test to help individuals identify mutations in the NIN gene associated with Seckel syndrome type 7. This rare genetic disorder is characterized by growth delays, microcephaly (small head size), and intellectual disability.

Test Details

The NIN Gene Seckel syndrome type 7 NGS Genetic Test utilizes Next-Generation Sequencing (NGS) technology, which allows for the analysis of multiple genes simultaneously. By sequencing the DNA of an individual, we can identify any variations or mutations in the NIN gene that may be causing the symptoms of Seckel syndrome type 7.

Components

  • Test Name: NIN Gene Seckel syndrome type 7 Genetic Test
  • 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 NIN Gene Seckel syndrome type 7 NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by Seckel syndrome type 7.

Benefits of the NGS Genetic Test

The NGS Genetic Test can provide a definitive diagnosis for individuals suspected to have Seckel syndrome type 7. The results can guide medical management and treatment options. Additionally, the test offers valuable information for genetic counseling and family planning purposes.

It is important to note that genetic testing is not always necessary or appropriate for everyone. The decision to undergo testing should be made in consultation with a healthcare professional or genetic counselor.

Test Name NIN Gene Seckel syndrome type 7 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 NIN Gene Seckel syndrome type 7 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NIN Gene Seckel syndrome type 7 NGS Genetic DNA Test gene NIN
Test Details

NIN Gene Seckel syndrome type 7 NGS Genetic Test is a type of genetic test that is used to identify mutations in the NIN gene that are associated with Seckel syndrome type 7. Seckel syndrome is a rare genetic disorder characterized by growth delays, small head size (microcephaly), and intellectual disability. There are several different types of Seckel syndrome, each caused by mutations in different genes.

The NGS (Next-Generation Sequencing) Genetic Test is a high-throughput sequencing method that allows for the analysis of multiple genes simultaneously. It involves sequencing the DNA of an individual to identify any variations or mutations in the NIN gene that may be causing the symptoms of Seckel syndrome type 7. This test can help provide a definitive diagnosis for individuals suspected to have this specific type of Seckel syndrome.

The results of the NGS Genetic Test can be used to guide medical management and treatment options for individuals with Seckel syndrome type 7. It can also provide valuable information for genetic counseling and family planning purposes. However, it is important to note that genetic testing is not always necessary or appropriate for everyone, and the decision to undergo testing should be made in consultation with a healthcare professional or genetic counselor.

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