TCTN1 Gene Joubert Syndrome Type 13 Genetic Test sale cost 4400 AED
CNKSR2 Gene Intellectual Disability Nonsyndromic CNKSR2 Related Genetic Test sale cost 4400 AED CNKSR2 Gene Intellectual Disability Nonsyndromic CNKSR2 Related 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!

TCTN1 Gene Joubert Syndrome Type 13 Genetic Test Cost

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

-21%

The TCTN1 gene Joubert Syndrome Type 13 genetic test is a specialized diagnostic tool designed to identify mutations in the TCTN1 gene, which are associated with Joubert Syndrome Type 13. This rare genetic disorder is characterized by a variety of symptoms, including developmental delays, coordination problems, abnormal eye movements, and the distinctive “molar tooth sign” visible on brain imaging. Early and accurate diagnosis through genetic testing can aid in the management of symptoms and the provision of appropriate care and interventions.

The test is conducted at DNA Labs UAE, a leading facility in genetic diagnostics, ensuring high accuracy and reliability of results. The cost of the test is 4400 AED, reflecting the comprehensive analysis and expertise required to identify the specific genetic alterations linked to this condition. This test is crucial for families seeking to understand their genetic health, enabling informed decisions regarding treatment and support for affected individuals.

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

TCTN1 Gene Joubert syndrome type 13 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 TCTN1 Gene Joubert syndrome type 13 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TCTN1 Gene Joubert syndrome type 13.

Test Details:

The TCTN1 gene is associated with Joubert syndrome type 13, a rare genetic disorder that affects the development of the brain. Joubert syndrome is characterized by abnormal breathing patterns, impaired coordination, intellectual disability, and other neurological abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual. It allows for the simultaneous sequencing of multiple genes, including the TCTN1 gene, to identify any variations or mutations that may be present. This type of testing can help diagnose Joubert syndrome type 13 and provide information about the specific genetic cause of the disorder.

If you suspect that you or someone you know may have Joubert syndrome type 13, a healthcare professional can order a NGS genetic test to confirm the diagnosis. The test involves collecting a sample of blood or saliva, which is then sent to a laboratory for analysis. The results of the test can help guide treatment and management strategies for individuals with Joubert syndrome type 13.

Test Name TCTN1 Gene Joubert syndrome type 13 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 TCTN1 Gene Joubert syndrome type 13 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TCTN1 Gene Joubert syndrome type 13
Test Details

The TCTN1 gene is associated with Joubert syndrome type 13, a rare genetic disorder that affects the development of the brain. Joubert syndrome is characterized by abnormal breathing patterns, impaired coordination, intellectual disability, and other neurological abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual. It allows for the simultaneous sequencing of multiple genes, including the TCTN1 gene, to identify any variations or mutations that may be present. This type of testing can help diagnose Joubert syndrome type 13 and provide information about the specific genetic cause of the disorder.

If you suspect that you or someone you know may have Joubert syndrome type 13, a healthcare professional can order a NGS genetic test to confirm the diagnosis. The test involves collecting a sample of blood or saliva, which is then sent to a laboratory for analysis. The results of the test can help guide treatment and management strategies for individuals with Joubert syndrome type 13.

SKU: TEST-1452