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Angelman Syndrome Test

Original price was: 1,870 د.إ.Current price is: 1,680 د.إ.

-10%

Angelman Syndrome Test at DNA Labs UAE is a specialized diagnostic procedure aimed at identifying Angelman Syndrome, a genetic disorder that primarily affects the nervous system, leading to developmental delays, problems with speech and balance, intellectual disability, and sometimes, seizures. Priced at 1680 AED, this test focuses on detecting abnormalities or mutations in the UBE3A gene located on chromosome 15, which are responsible for the syndrome. The testing process involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the state-of-the-art facilities of DNA Labs UAE. The results of this test can provide crucial information for the diagnosis, management, and understanding of Angelman Syndrome, offering families and healthcare providers valuable insights into the condition and potential treatment or intervention strategies.

Home  Sample collection service available

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  • This test is not intended for medical diagnosis or treatment
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ANGELMAN SYNDROME Test Cost AED: 1680.0

Angelman syndrome is a neurologic disorder characterized by developmental delay, intellectual disability, speech impairment, and characteristic behavioral traits. DNA Labs UAE offers a comprehensive genetic test for Angelman syndrome to confirm the diagnosis.

Test Details

There is no specific test for Angelman syndrome. Diagnosis is typically based on clinical features. However, genetic testing can confirm the diagnosis by identifying a deletion or mutation in the UBE3A gene, which is responsible for Angelman syndrome.

The DNA methylation test is one method used for genetic testing. It involves analyzing the methylation pattern of the UBE3A gene. Another method is chromosomal microarray analysis, which can detect deletions or duplications in the 15q11-q13 region of chromosome 15.

In some cases, a fluorescence in situ hybridization (FISH) test may be performed to detect a deletion in the 15q11-q13 region of chromosome 15.

Test Components and Price

The ANGELMAN SYNDROME Test is priced at 1680.0 AED. The test requires a sample condition of 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. The sample should be shipped refrigerated and should not be frozen. A duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory for the test.

Report Delivery

The sample should be received by 11 am, and the report will be delivered within 12 working days.

Test Type and Doctor

The ANGELMAN SYNDROME Test falls under the category of Neurologic Disorder. The test is conducted by Neurologists, Physicians, and Pediatricians in the Molecular Diagnostics department.

Pre Test Information

A duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory for the test.

Test Name ANGELMAN SYNDROME Test
Components
Price 1680.0 AED
Sample Condition 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Report Delivery SampleSat by 11 am; Report 12 Working days
Method Methylation specific PCR
Test type Neurologic Disorder
Doctor Neurologist, Physician, Pediatrician
Test Department: MOLECULAR DIAGNOSTICS
Pre Test Information Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Test Details

There is no specific test for Angelman syndrome. Diagnosis is typically based on clinical features, such as developmental delay, intellectual disability, speech impairment, and characteristic behavioral traits. Genetic testing, specifically a DNA methylation test or a chromosomal microarray analysis, can confirm the diagnosis by identifying a deletion or mutation in the UBE3A gene, which is responsible for Angelman syndrome. In some cases, a fluorescence in situ hybridization (FISH) test may be performed to detect a deletion in the 15q11-q13 region of chromosome 15.

SKU: TEST-5223 Category:

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