Sale!

EXOC8 Gene Joubert syndrome EXOC8 related Genetic Test

4,400 د.إ

-21%

The EXOC8 gene is associated with Joubert syndrome, a rare genetic disorder characterized by the malformation of the cerebellum and brainstem, leading to a range of developmental delays and neurological issues. The disorder falls under a group of conditions known as ciliopathies, which are caused by defects in the structure or function of cilia, the microscopic cellular antennae vital for communication and signaling.

Given the genetic basis of Joubert syndrome, identifying mutations in genes like EXOC8 is crucial for diagnosis, understanding the disease’s progression, and potential management strategies. The EXOC8-related genetic test is a sophisticated diagnostic tool designed to detect mutations in the EXOC8 gene, thereby confirming the diagnosis of Joubert syndrome and assisting in the formulation of a personalized treatment plan.

This specific genetic test is available at DNA Labs UAE, a facility renowned for its advanced genetic testing services. The cost of the EXOC8 gene test is set at 4400 AED. This investment covers the collection of a DNA sample, usually through a blood draw or cheek swab, the analysis of the EXOC8 gene for any mutations, and a comprehensive report that interprets the findings. Given the complexity of genetic disorders like Joubert syndrome, the availability of such targeted genetic testing is invaluable for affected families, offering them insights into the condition and guiding them towards appropriate medical and supportive care.

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

EXOC8 Gene Joubert Syndrome Genetic Test

Welcome to DNA Labs UAE, your trusted genetic testing laboratory. Today, we will be discussing the EXOC8 gene and its relation to Joubert syndrome. Additionally, we will provide detailed information about the EXOC8-related genetic test, including its cost, symptoms, diagnosis, and more.

Test Name: EXOC8 Gene Joubert Syndrome EXOC8-related Genetic Test

Components: This test analyzes the EXOC8 gene to identify any mutations or variations that may be contributing to the development of Joubert syndrome.

Price: AED 4400.0

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: Before undergoing the EXOC8 Gene Joubert Syndrome EXOC8-related NGS Genetic DNA 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 Joubert syndrome.

About Joubert Syndrome and the EXOC8 Gene

Joubert syndrome is a rare genetic disorder that affects the development of the brain. It is characterized by a distinctive brain malformation called the “molar tooth sign,” which can be seen on brain imaging scans. The EXOC8 gene is associated with Joubert syndrome.

NGS Genetic Testing for Joubert Syndrome

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously, providing a comprehensive evaluation of genetic variations. In the case of Joubert syndrome, an EXOC8-related NGS genetic test involves sequencing the EXOC8 gene to identify any mutations or variations that may be contributing to the development of the disorder.

This type of genetic testing can help confirm a diagnosis of Joubert syndrome and provide valuable information for genetic counseling and family planning. It may also be useful for identifying individuals who are carriers of EXOC8 gene mutations but do not show symptoms of the disorder themselves.

It’s important to note that genetic testing for Joubert syndrome and other genetic disorders should be done under the guidance of a healthcare professional or genetic counselor who can help interpret the results and provide appropriate recommendations and support.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. If you have any questions or would like to schedule an appointment for the EXOC8 Gene Joubert Syndrome EXOC8-related Genetic Test, please contact our laboratory.

Test Name EXOC8 Gene Joubert syndrome EXOC8 related 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 EXOC8 Gene Joubert syndrome, EXOC8 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with EXOC8 Gene Joubert syndrome, EXOC8 related
Test Details

The EXOC8 gene is associated with Joubert syndrome, a rare genetic disorder that affects the development of the brain. Joubert syndrome is characterized by a distinctive brain malformation called the “molar tooth sign,” which can be seen on brain imaging scans.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously, providing a comprehensive evaluation of genetic variations. In the case of Joubert syndrome, an EXOC8-related NGS genetic test would involve sequencing the EXOC8 gene to identify any mutations or variations that may be contributing to the development of the disorder.

This type of genetic testing can help confirm a diagnosis of Joubert syndrome and provide valuable information for genetic counseling and family planning. It may also be useful for identifying individuals who are carriers of EXOC8 gene mutations but do not show symptoms of the disorder themselves.

It’s important to note that genetic testing for Joubert syndrome and other genetic disorders should be done under the guidance of a healthcare professional or genetic counselor who can help interpret the results and provide appropriate recommendations and support.