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Chromosome Analysis High Resolution Neonatal Test

870 د.إ

-9%

Chromosome Analysis High Resolution Neonatal Test is a comprehensive diagnostic procedure aimed at detecting chromosomal abnormalities in newborns with unparalleled accuracy. This high-resolution test examines the chromosomes in detail, allowing for the identification of structural changes and anomalies that could be linked to a variety of genetic disorders. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test ensures a thorough analysis, providing crucial information for early intervention and management of potential genetic conditions. The cost of the test is 870 AED, making it an accessible option for parents seeking peace of mind regarding their newborn’s genetic health. With state-of-the-art technology and expert analysis, DNA Labs UAE offers reliable results, contributing to the effective care and well-being of neonates.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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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.