CHROMOSOME ANALYSIS HIGH RESOLUTION NEONATAL Test
Test Cost: AED 870.0
Test Components:
- Price: 870.0 AED
- Sample Condition: 4 ml (2 ml min). whole blood in 1 Green top (Sodium Heparin ) tube. Ship refrigerated immediately. DO NOT FREEZE.
Report Delivery:
Sample Daily by 6 pm; Report 21 Working days
Method:
Culture, Microscopy, High Resolution Karyotype
Test Type:
Genetic Disorders
Doctor:
Pediatrician
Test Department:
CYTOGENETICS
Pre Test Information:
Test is recommended between 18-20 weeks of gestation. Duly filled Chromosome & FISH Analysis Requisition form (Form 17) is mandatory.
Test Details:
Chromosome analysis, also known as karyotyping, is a test that examines the number, size, and shape of chromosomes in a person’s cells. This test can help identify any abnormalities or genetic disorders that may be present. High-resolution chromosome analysis specifically refers to a more detailed examination of the chromosomes, allowing for a better view of the genetic material.
This type of analysis is often used in neonatal testing, which is performed on newborn babies to screen for any genetic abnormalities or disorders that may be present at birth. Neonatal chromosome analysis is typically recommended when there are physical abnormalities or developmental delays in a newborn, or if there is a family history of genetic disorders.
The test involves obtaining a sample of cells, usually through a blood sample, and then examining the chromosomes under a microscope. The high-resolution aspect of the test allows for a more accurate analysis of the chromosomes, which can help detect smaller abnormalities or genetic changes that may not be visible with a standard karyotype. This can be particularly important in identifying certain genetic disorders that may have subtle or complex chromosome changes.
Overall, high-resolution neonatal chromosome analysis is a valuable tool in diagnosing and managing genetic disorders in newborns, providing important information for healthcare professionals and families to make informed decisions about treatment and support.
Test Name | CHROMOSOME ANALYSIS HIGH RESOLUTION NEONATAL Test |
---|---|
Components | |
Price | 870.0 AED |
Sample Condition | 4 ml (2 ml min). whole blood in 1 Green top (Sodium Heparin ) tube.Ship refrigerated immediately. DO NOT FREEZE. Test is recommended between 18-20 weeks of gestation. Duly filledChromosome & FISH Analysis Requisition form (Form 17)is mandatory. |
Report Delivery | Sample Daily by 6 pm; Report 21 Working days |
Method | Culture, Microscopy, High Resolution Karyotype |
Test type | Genetic Disorders |
Doctor | Pediatrician |
Test Department: | CYTOGENETICS |
Pre Test Information | Test is recommended between 18-20 weeks of gestation. Duly filledChromosome & FISH Analysis Requisition form (Form 17)is mandatory. |
Test Details | Chromosome analysis, also known as karyotyping, is a test that examines the number, size, and shape of chromosomes in a person’s cells. This test can help identify any abnormalities or genetic disorders that may be present. High-resolution chromosome analysis specifically refers to a more detailed examination of the chromosomes, allowing for a better view of the genetic material. This type of analysis is often used in neonatal testing, which is performed on newborn babies to screen for any genetic abnormalities or disorders that may be present at birth. Neonatal chromosome analysis is typically recommended when there are physical abnormalities or developmental delays in a newborn, or if there is a family history of genetic disorders. The test involves obtaining a sample of cells, usually through a blood sample, and then examining the chromosomes under a microscope. The high-resolution aspect of the test allows for a more accurate analysis of the chromosomes, which can help detect smaller abnormalities or genetic changes that may not be visible with a standard karyotype. This can be particularly important in identifying certain genetic disorders that may have subtle or complex chromosome changes. Overall, high-resolution neonatal chromosome analysis is a valuable tool in diagnosing and managing genetic disorders in newborns, providing important information for healthcare professionals and families to make informed decisions about treatment and support. |