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CDKL5 Gene Angelman-like syndrome Genetic Test

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

-21%

The CDKL5 Gene Angelman-like Syndrome Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the CDKL5 gene. These mutations are known to cause a rare genetic disorder that presents with symptoms similar to Angelman syndrome, including developmental delays, intellectual disabilities, and epilepsy. The test, which costs 4400 AED, involves analyzing the patient’s DNA to detect abnormalities in the CDKL5 gene, providing crucial information for accurate diagnosis and management of the condition. This test is a critical step for families seeking answers to complex neurological symptoms, guiding them towards appropriate treatments and support services.

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CDKL5 Gene Angelman-like Syndrome Genetic Test

At DNA Labs UAE, we offer the CDKL5 Gene Angelman-like Syndrome Genetic Test for individuals who may be experiencing symptoms related to this rare genetic disorder. This diagnostic test utilizes next-generation sequencing (NGS) technology to analyze the CDKL5 gene for mutations or variations that may cause Angelman-like syndrome.

What is Angelman-like Syndrome?

Angelman-like syndrome is a rare genetic disorder that shares many clinical features with Angelman syndrome. These features include developmental delay, intellectual disability, seizures, and speech impairment. However, Angelman-like syndrome is specifically caused by mutations in the CDKL5 gene, which is located on the X chromosome.

How Does the CDKL5 Gene Angelman-like Syndrome Genetic Test Work?

The CDKL5 gene provides instructions for making a protein that is crucial for brain development and function. Mutations in this gene can disrupt the normal functioning of the protein, leading to the symptoms associated with Angelman-like syndrome. Our NGS-based genetic test analyzes the CDKL5 gene to identify any mutations or variations that may be present.

Test Components and Price

The CDKL5 Gene Angelman-like Syndrome Genetic Test is priced at 4400.0 AED. The test can be conducted using a blood sample, extracted DNA, or one drop of blood on an FTA card.

Test Method and Type

The test utilizes NGS technology to analyze the CDKL5 gene for mutations or variations. It falls under the category of neurological disorders, specifically targeting Angelman-like syndrome.

Test Department and Doctor

The CDKL5 Gene Angelman-like Syndrome Genetic Test is conducted by our Genetics department, under the supervision of a Neurologist.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is undergoing the CDKL5 Gene Angelman-like Syndrome NGS Genetic DNA Test. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by CDKL5 Gene Angelman-like Syndrome.

Report Delivery

Once the test is conducted, the report will be delivered within 3 to 4 weeks.

Conclusion

The CDKL5 Gene Angelman-like Syndrome Genetic Test offered by DNA Labs UAE is a valuable diagnostic tool for identifying mutations or variations in the CDKL5 gene that may be causing Angelman-like syndrome. This test can aid in the diagnosis of the condition and guide treatment decisions.

Test Name CDKL5 Gene Angelman-like syndrome 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 CDKL5 Gene Angelman-like syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CDKL5 Gene Angelman-like syndrome
Test Details

CDKL5 gene Angelman-like syndrome NGS genetic test is a diagnostic test that uses next-generation sequencing (NGS) technology to analyze the CDKL5 gene for mutations or variations that may cause Angelman-like syndrome. Angelman-like syndrome is a rare genetic disorder that shares many of the clinical features of Angelman syndrome, including developmental delay, intellectual disability, seizures, and speech impairment. However, unlike Angelman syndrome, Angelman-like syndrome is caused by mutations in the CDKL5 gene, which is located on the X chromosome. The CDKL5 gene provides instructions for making a protein that is important for brain development and function. Mutations in this gene can disrupt the normal functioning of the protein, leading to the symptoms of Angelman-like syndrome. The CDKL5 gene Angelman-like syndrome NGS genetic test can help diagnose the condition and guide treatment decisions.