TCTN3 Gene Joubert Syndrome Type 18 Genetic Test sale cost 4400 AED
MYH2 Gene Inclusion Body Myopathy Genetic Test sale cost 4400 AED MYH2 Gene Inclusion Body Myopathy Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
ROGDI Gene Kohlschutter Tonz syndrome Genetic Test sale cost 4400 AED ROGDI Gene Kohlschutter Tonz syndrome Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
Sale!

TCTN3 Gene Joubert Syndrome Type 18 Genetic Test Cost

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

-21%

The TCTN3 Gene Joubert Syndrome Type 18 Genetic Test is a specialized diagnostic examination available at DNA Labs UAE, designed to identify mutations in the TCTN3 gene, which are implicated in the development of Joubert Syndrome Type 18. This rare genetic disorder is characterized by a range of symptoms, including developmental delays, coordination issues, and distinctive structural brain abnormalities known as the “molar tooth sign” on MRI scans. The test, priced at 4400 AED, involves analyzing the patient’s DNA to detect mutations in the TCTN3 gene, providing crucial information for diagnosis, treatment planning, and genetic counseling for affected families. By offering this test, DNA Labs UAE provides a valuable resource for individuals and families seeking answers about this rare condition, facilitating early intervention and personalized care strategies.

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
Guaranteed Safe Checkout

TCTN3 Gene Joubert Syndrome Type 18 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: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for TCTN3 Gene Joubert syndrome type 18 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TCTN3 Gene Joubert syndrome type 18.

Test Details

The TCTN3 gene is associated with Joubert syndrome type 18, which is a rare genetic disorder characterized by developmental delay, intellectual disability, breathing abnormalities, and distinctive facial features. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of Joubert syndrome type 18, NGS genetic testing can be used to analyze the TCTN3 gene for any mutations or variations that may be causing the disorder. NGS genetic testing involves sequencing the DNA of an individual to identify any changes or variations in the genes of interest. This can help in confirming a diagnosis, understanding the genetic basis of the disorder, and providing information for genetic counseling and family planning. It is important to consult with a healthcare professional or genetic counselor to discuss the appropriateness and availability of NGS genetic testing for Joubert syndrome type 18 and to understand the potential implications of the test results.

Test Name TCTN3 Gene Joubert syndrome type 18 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for TCTN3 Gene Joubert syndrome type 18 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TCTN3 Gene Joubert syndrome type 18
Test Details

The TCTN3 gene is associated with Joubert syndrome type 18, which is a rare genetic disorder characterized by developmental delay, intellectual disability, breathing abnormalities, and distinctive facial features.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of Joubert syndrome type 18, NGS genetic testing can be used to analyze the TCTN3 gene for any mutations or variations that may be causing the disorder.

NGS genetic testing involves sequencing the DNA of an individual to identify any changes or variations in the genes of interest. This can help in confirming a diagnosis, understanding the genetic basis of the disorder, and providing information for genetic counseling and family planning.

It is important to consult with a healthcare professional or genetic counselor to discuss the appropriateness and availability of NGS genetic testing for Joubert syndrome type 18 and to understand the potential implications of the test results.

SKU: TEST-1457 Category:

Related products