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Newborns Genetic Test Panel NGS Genetic Test Cost

Original price was: 6,000 د.إ.Current price is: 4,400 د.إ.

-27%

The “Newborns Genetic Test Panel NGS (Next Generation Sequencing) Genetic Test” is an advanced genetic screening procedure offered by DNA Labs UAE, designed to identify genetic disorders in newborns. This comprehensive test, priced at 4400 AED, utilizes the latest NGS technology to analyze the baby’s DNA, covering a wide range of genetic conditions that could affect a child’s health. By examining the genetic material, the test can pinpoint mutations or changes in genes that may lead to diseases or conditions, enabling early detection and intervention. This early diagnostic approach allows for timely management and treatment options, potentially improving the quality of life for affected infants. Conducted in the state-of-the-art facilities of DNA Labs UAE, this test represents a crucial step forward in neonatal care, offering parents peace of mind and the necessary information to prepare for and address any health challenges their newborn might face.

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  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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Newborns Genetic Test Panel NGS Genetic Test

Are you concerned about your newborn baby’s health? DNA Labs UAE offers the Newborns Genetic Test Panel NGS Genetic Test to screen newborns for a range of genetic disorders. With a comprehensive analysis of your baby’s DNA, this test can provide valuable information about their health.

Test Name: Newborns Genetic Test Panel NGS Genetic DNA Test

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test Type: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information

Before undergoing the Newborns Genetic Test Panel NGS Genetic DNA Test, it is important to provide the clinical history of the patient. A Genetic Counselling session may be conducted to draw a pedigree chart of family members affected with the Newborns Genetic Test Panel.

Test Details

The Newborns Genetic Test Panel is a Next-Generation Sequencing (NGS) genetic DNA test that screens newborn babies for a range of genetic disorders. This test involves analyzing the baby’s DNA for specific genetic mutations or variations associated with inherited diseases and conditions.

The test is typically performed within the first few days of a baby’s life, using a small blood sample collected from a heel prick. The sample is then sent to a laboratory for analysis, where the DNA is extracted and sequenced using advanced genetic testing technology.

The Newborns Genetic Test Panel includes screening for various genetic disorders such as metabolic disorders, cystic fibrosis, sickle cell anemia, and other inherited conditions. The results of the test can help identify potential health risks or conditions that may require early intervention or treatment.

Overall, the Newborns Genetic Test Panel is a valuable tool for identifying potential health risks in newborns and providing parents with important information about their baby’s health.

 

Test NameNewborns Genetic Test Panel NGS Genetic DNA Test
Components 
Price4400.0 AED
Sample ConditionBlood or Extracted DNA or One drop Blood on FTA Card
Report Delivery3 to 4 Weeks
MethodNGS Technology
Test typeMetabolic Disorders
DoctorGeneral Physician
Test Department:Genetics
Pre Test InformationClinical History of Patient who is going for Newborns Genetic Test Panel NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Newborns Genetic Test Panel
Test Details

The Newborns Genetic Test Panel is a type of Next-Generation Sequencing (NGS) genetic DNA test that is used to screen newborn babies for a range of genetic disorders. This test involves analyzing the baby’s DNA for specific genetic mutations or variations that are associated with various inherited diseases and conditions.

The Newborns Genetic Test Panel is typically performed within the first few days of a baby’s life, using a small blood sample collected from a heel prick. The sample is then sent to a laboratory for analysis, where the DNA is extracted and sequenced using advanced genetic testing technology.

The test panel typically includes screening for a range of genetic disorders, including metabolic disorders, cystic fibrosis, sickle cell anemia, and various other inherited conditions. The results of the test can help identify any potential health risks or conditions that may require early intervention or treatment.

Overall, the Newborns Genetic Test Panel is a valuable tool for identifying potential health risks in newborns and providing parents with important information about their baby’s health.

SKU: TEST-849 Category:

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