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 Name | CentoIEM NGS Genetic DNA Test |
---|---|
Components | |
Price | 4400.0 AED |
Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Neurological Disorders |
Doctor | Neurologist |
Test Department: | Genetics |
Pre Test Information | Clinical 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. |