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CentoIEM NGS Genetic Test

4,400 د.إ

-27%

The CentoIEM NGS Genetic Test, available at DNA Labs UAE, is a comprehensive genetic testing solution designed to detect a wide range of inherited metabolic disorders. Utilizing Next-Generation Sequencing (NGS) technology, this test offers a highly accurate and efficient approach to identifying genetic variations associated with metabolic conditions. With a cost of 4400 AED, the CentoIEM NGS Genetic Test is a valuable tool for clinicians and patients aiming to understand genetic predispositions and tailor personalized treatment plans. By analyzing a patient’s DNA, the test can provide insights into more than 100 different metabolic disorders, enabling early detection and intervention, which is crucial for managing these conditions effectively. DNA Labs UAE, with its state-of-the-art facilities and expert team, ensures reliable results and comprehensive support throughout the testing process.

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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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CentoIEM NGS Genetic Test – Cost, Symptoms, Diagnosis

Welcome to DNA Labs UAE, a leading genetic laboratory specializing in DNA testing. In this blog post, we will discuss the CentoIEM NGS Genetic Test, its cost, symptoms, and diagnosis process.

Test Name: CentoIEM NGS Genetic DNA Test

Components: 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: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information

Before undergoing the CentoIEM 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 CentoIEM.

Test Details

The CentoIEM NGS Genetic DNA Test is a diagnostic tool used to identify genetic mutations that cause inborn errors of metabolism (IEM). It utilizes next-generation sequencing (NGS) technology to analyze a patient’s DNA and identify variants in genes associated with IEMs.

IEMs are rare genetic disorders that affect the body’s ability to process certain nutrients, leading to a range of symptoms and health problems. Early detection of these disorders is crucial for effective treatment.

The CentoIEM NGS Genetic DNA Test can detect over 300 genetic variants associated with IEMs, including amino acid disorders, organic acid disorders, fatty acid oxidation disorders, and others. It can be used for diagnosing patients with suspected IEMs, as well as screening newborns for these disorders.

The test is performed on a blood or saliva sample, and results are typically available within a few weeks. Positive results are confirmed with additional testing, and patients with confirmed diagnoses may be referred to specialists for treatment and management.

Overall, the CentoIEM NGS Genetic DNA Test is a valuable tool for diagnosing and managing IEMs, contributing to improved outcomes for patients with these rare and challenging disorders.

 

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

The CentoIEM NGS Genetic DNA Test is a diagnostic tool used to identify genetic mutations that cause inborn errors of metabolism (IEM). It uses next-generation sequencing (NGS) technology to analyze a patient’s DNA and identify variants in genes associated with IEMs.

IEMs are rare genetic disorders that affect the body’s ability to process certain nutrients, leading to a range of symptoms and health problems. These disorders can be difficult to diagnose, and early detection is critical for effective treatment.

The CentoIEM NGS Genetic DNA Test can detect over 300 genetic variants associated with IEMs, including amino acid disorders, organic acid disorders, fatty acid oxidation disorders, and others. It can be used to diagnose patients with suspected IEMs, as well as to screen newborns for these disorders.

The test is performed on a blood or saliva sample, and results are typically available within a few weeks. Positive results are confirmed with additional testing, and patients with confirmed diagnoses may be referred to specialists for treatment and management.

Overall, the CentoIEM NGS Genetic DNA Test is a valuable tool for diagnosing and managing IEMs, helping to improve outcomes for patients with these rare and challenging disorders.