CNTNAP4 Gene Neurodevelopmental Disorder
At DNA Labs UAE, we offer the CNTNAP4 Gene Neurodevelopmental Disorder genetic test to diagnose and provide information about this disorder. The test is priced at AED 4400.0 and requires a blood sample, extracted DNA, or one drop of blood on an FTA card. The test results are typically delivered within 3 to 4 weeks.
Test Details
The CNTNAP4 gene is associated with a neurodevelopmental disorder called CNTNAP4-related NGS (Next-Generation Sequencing) Genetic Test. This disorder is characterized by various neurological and developmental problems.
The CNTNAP4 gene provides instructions for making a protein called contactin-associated protein-like 4 (CNTNAP4). This protein is involved in the development and function of neurons in the brain. Mutations or changes in the CNTNAP4 gene can disrupt the normal functioning of the protein, leading to abnormal brain development and function.
Individuals with CNTNAP4-related neurodevelopmental disorder may experience symptoms such as intellectual disability, developmental delay, speech and language difficulties, autism spectrum disorder, and epilepsy.
Test Process
The CNTNAP4-related NGS Genetic Test utilizes next-generation sequencing technology to analyze the DNA sequence of the CNTNAP4 gene. By identifying mutations or changes in the gene, this test can confirm a diagnosis of CNTNAP4-related neurodevelopmental disorder and provide information about the specific genetic changes involved.
Test Department and Doctor
This genetic test is conducted in our Genetics department and overseen by a Neurologist. Our team of experts ensures accurate and reliable results.
Pre-Test Information
Prior to the test, it is important to provide the clinical history of the patient who is undergoing the CNTNAP4 Gene Neurodevelopmental Disorder genetic test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by the disorder.
Conclusion
The CNTNAP4 Gene Neurodevelopmental Disorder genetic test offered at DNA Labs UAE is an essential tool in diagnosing and managing this disorder. By analyzing the DNA sequence of the CNTNAP4 gene, this test provides valuable information for genetic counseling and treatment strategies.
Test Name | CNTNAP4 Gene Neurodevelopmental disorder CNTNAP4 related Genetic Test |
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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 CNTNAP4 Gene Neurodevelopmental disorder, CNTNAP4 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CNTNAP4 Gene Neurodevelopmental disorder, CNTNAP4 related |
Test Details |
The CNTNAP4 gene is associated with a neurodevelopmental disorder called CNTNAP4-related NGS (Next-Generation Sequencing) Genetic Test. This disorder is characterized by various neurological and developmental problems. The CNTNAP4 gene provides instructions for making a protein called contactin-associated protein-like 4 (CNTNAP4). This protein is involved in the development and function of neurons in the brain. Mutations or changes in the CNTNAP4 gene can disrupt the normal functioning of the protein, leading to abnormal brain development and function. This can result in a range of symptoms, including intellectual disability, developmental delay, speech and language difficulties, autism spectrum disorder, and epilepsy. The CNTNAP4-related NGS Genetic Test is a diagnostic test that uses next-generation sequencing technology to analyze the DNA sequence of the CNTNAP4 gene. It can identify mutations or changes in the gene that may be causing the neurodevelopmental disorder. This genetic test can help in confirming a diagnosis of CNTNAP4-related neurodevelopmental disorder, as well as providing information about the specific genetic changes involved. This can be useful for genetic counseling and for guiding treatment and management strategies for individuals with this disorder. |