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CEP41 Gene Joubert Syndrome Type 15 Genetic Test

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

-21%

The CEP41 gene is associated with Joubert Syndrome Type 15 (JBTS15), a rare genetic disorder characterized by the malformation of the cerebellum and brain stem, leading to a range of neurological symptoms, including coordination and balance issues, abnormal eye movements, and developmental delays. Genetic testing for mutations in the CEP41 gene is crucial for the diagnosis of JBTS15, enabling healthcare providers to offer accurate prognoses, personalized treatment plans, and genetic counseling for affected families.

DNA Labs UAE offers a specialized genetic test targeting the CEP41 gene to diagnose Joubert Syndrome Type 15. The test involves analyzing the patient’s DNA to identify mutations in the CEP41 gene that are known to cause the condition. This test is vital for confirming the diagnosis of JBTS15, particularly in individuals showing the syndrome’s characteristic symptoms or with a family history of the condition.

The cost of the CEP41 gene test for Joubert Syndrome Type 15 at DNA Labs UAE is 4400 AED. This price includes the full genetic analysis and a comprehensive report that can be used by healthcare professionals to guide treatment and management decisions for the patient. It is important for individuals considering this test to consult with a genetic counselor or healthcare provider to understand the implications of the results and the next steps in care and management.

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CEP41 Gene Joubert Syndrome Type 15 Genetic Test

Test Name: CEP41 Gene Joubert Syndrome Type 15 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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 CEP41 Gene Joubert Syndrome Type 15 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CEP41 Gene Joubert Syndrome Type 15.

Test Details

The CEP41 gene is associated with Joubert syndrome type 15, a rare genetic disorder characterized by developmental delay, intellectual disability, abnormal breathing patterns, and a specific brain malformation known as the “molar tooth sign.”

NGS (Next-Generation Sequencing) Genetic Testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Joubert syndrome type 15, NGS genetic testing can be used to identify mutations or variations in the CEP41 gene that may be responsible for the disorder.

This type of genetic testing can help in confirming a clinical diagnosis, providing information on the specific genetic cause of the disorder, and assessing the risk of passing the condition on to future generations. It can also be used for carrier testing in individuals with a family history of Joubert syndrome type 15.

It is important to note that genetic testing should be performed and interpreted by healthcare professionals with expertise in genetics, as the results can have significant implications for individuals and their families. Genetic counseling is often recommended before and after genetic testing to discuss the benefits, limitations, and potential implications of the test results.

Test Name CEP41 Gene Joubert syndrome type 15 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 CEP41 Gene Joubert syndrome type 15 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CEP41 Gene Joubert syndrome type 15
Test Details

The CEP41 gene is associated with Joubert syndrome type 15, a rare genetic disorder characterized by developmental delay, intellectual disability, abnormal breathing patterns, and a specific brain malformation known as the “molar tooth sign.”

NGS (Next-Generation Sequencing) Genetic Testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Joubert syndrome type 15, NGS genetic testing can be used to identify mutations or variations in the CEP41 gene that may be responsible for the disorder.

This type of genetic testing can help in confirming a clinical diagnosis, providing information on the specific genetic cause of the disorder, and assessing the risk of passing the condition on to future generations. It can also be used for carrier testing in individuals with a family history of Joubert syndrome type 15.

It is important to note that genetic testing should be performed and interpreted by healthcare professionals with expertise in genetics, as the results can have significant implications for individuals and their families. Genetic counseling is often recommended before and after genetic testing to discuss the benefits, limitations, and potential implications of the test results.