CHROMOFIC KARYOARRAY Test
Test Name: CHROMOFIC KARYOARRAY Test
Components: Blood samples (4 mL whole blood in 1 Lavender Top (EDTA) tube and 4 mL whole blood in 1 Green Top (Sodium Heparin) tube)
Price: 5850.0 AED
Sample Condition: Ship refrigerated. DO NOT FREEZE.
Required Form: Duly filled Genomic Microarray Requisition form (Form 19)
Report Delivery: Sample daily by 4 pm; Report within 10 working days
Method: Affymetrix CytoScan 750K microarray and Microscopy
Test Type: Disorders of Nervous System
Doctor: Pediatrician
Test Department: CYTOGENETICS
Pre Test Information:
The CHROMOFIC KARYOARRAY test is a genetic test that analyzes a person’s chromosomes for abnormalities. It uses a microarray technology that can detect small changes in the DNA structure, such as deletions, duplications, and rearrangements. The test is used to diagnose genetic disorders and to identify the cause of developmental delays, intellectual disabilities, and birth defects. It can also be used to determine the risk of passing on genetic conditions to future generations. The test is typically performed on a blood sample or other tissue sample and can take several weeks to complete.
Test Name | CHROMOFIC KARYOARRAY Test |
---|---|
Components | |
Price | 5850.0 AED |
Sample Condition | 4 mL (2 mL min.) whole blood in 1 Lavender Top (EDTA) tube AND 4 mL (2 mL min.) whole blood in 1 Green Top (Sodium Heparin) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomic Microarray Requisition form (Form 19) is mandatory. |
Report Delivery | Sample Daily by 4 pm; Report 10 Working days |
Method | Affymetrix CytoScan 750K microarray and Microscopy |
Test type | Disorders of Nervous System |
Doctor | Pediatrician |
Test Department: | CYTOGENETICS |
Pre Test Information | |
Test Details | The CHROMOFIC KARYOARRAY test is a genetic test that analyzes a person’s chromosomes for abnormalities. It uses a microarray technology that can detect small changes in the DNA structure, such as deletions, duplications, and rearrangements. The test is used to diagnose genetic disorders and to identify the cause of developmental delays, intellectual disabilities, and birth defects. It can also be used to determine the risk of passing on genetic conditions to future generations. The test is typically performed on a blood sample or other tissue sample and can take several weeks to complete. |