Metabolic Disorders Wide Range Panel NGS Genetic Test
Are you concerned about the risk of metabolic disorders? DNA Labs UAE offers the Metabolic Disorders Wide Range Panel NGS Genetic Test to analyze an individual’s DNA for mutations associated with these disorders. Read on to learn more about the test, including its cost, symptoms, and diagnosis process.
Test Details
The Metabolic Disorders Wide Range Panel NGS Genetic DNA Test is a comprehensive genetic test that examines an individual’s DNA for mutations or changes in genes associated with metabolic disorders. Metabolic disorders occur due to disruptions in the body’s normal metabolic processes, leading to various symptoms and health problems.
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: Metabolic Disorders
- Doctor: General Physician
- Test Department: Genetics
Pre Test Information
Prior to undergoing the Metabolic Disorders Wide Range Panel NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to create a pedigree chart of family members affected by metabolic disorders.
Disorders Detected
The test can detect various metabolic disorders, including:
- Phenylketonuria (PKU)
- Maple syrup urine disease (MSUD)
- Homocystinuria
- Gaucher disease
- Fabry disease
- Niemann-Pick disease
- Pompe disease
- Mucopolysaccharidosis (MPS)
- Wilson disease
- Hemochromatosis
Why Take the Test?
If you or your healthcare provider suspect a metabolic disorder based on your symptoms or family history, the Metabolic Disorders Wide Range Panel NGS Genetic DNA Test can provide valuable insights. The results of the test can guide treatment and management strategies, as well as inform family planning decisions for individuals at risk of passing on a genetic mutation to their children.
Don’t wait to address your concerns about metabolic disorders. Contact DNA Labs UAE today to learn more about the Metabolic Disorders Wide Range Panel NGS Genetic DNA Test and take control of your health.
| Test Name | Metabolic Disorders Wide Range Panel 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 | Metabolic Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for Metabolic Disorders Wide Range Panel NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Metabolic Disorders Wide Range Panel |
| Test Details |
The Metabolic Disorders Wide Range Panel NGS Genetic DNA Test is a type of genetic test that analyzes an individual’s DNA for mutations or changes in genes that are associated with metabolic disorders. These disorders are caused by a disruption in the body’s normal metabolic processes, which can lead to a wide range of symptoms and health problems. The test uses next-generation sequencing (NGS) technology to analyze multiple genes at once, allowing for a comprehensive assessment of an individual’s risk for metabolic disorders. Some of the disorders that can be detected by this test include: – Phenylketonuria (PKU) – Maple syrup urine disease (MSUD) – Homocystinuria – Gaucher disease – Fabry disease – Niemann-Pick disease – Pompe disease – Mucopolysaccharidosis (MPS) – Wilson disease – Hemochromatosis The test is typically ordered by a healthcare provider if there is a suspicion of a metabolic disorder based on an individual’s symptoms or family history. The results of the test can help guide treatment and management strategies for individuals with these disorders, as well as inform family planning decisions for those at risk of passing on a genetic mutation to their children. |
