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Metabolic Disorders Wide Range Panel NGS Genetic Test

4,400 د.إ

-27%

The “Metabolic Disorders Wide Range Panel NGS (Next-Generation Sequencing) Genetic Test” is a comprehensive diagnostic tool offered by DNA Labs UAE, designed to identify a broad spectrum of inherited metabolic disorders. Priced at 4400 AED, this advanced genetic testing employs next-generation sequencing technology to analyze multiple genes simultaneously, providing a thorough examination of the genetic variations associated with a wide range of metabolic disorders.

Metabolic disorders are a group of conditions that occur due to abnormal chemical reactions in the body, affecting the body’s ability to convert food into energy. These disorders can lead to a buildup of toxic substances or a deficiency of critical substances, often resulting in serious health issues. The test targets genes linked to conditions such as amino acid disorders, fatty acid oxidation disorders, organic acidemias, and more, offering crucial insights for early detection, management, and treatment planning.

Conducted at DNA Labs UAE, a facility known for its state-of-the-art technology and expert staff, this test is a valuable resource for individuals and families seeking to understand their genetic predisposition to metabolic disorders. The results from this test can guide healthcare professionals in making informed decisions about patient care, including dietary recommendations, lifestyle changes, and potential interventions to prevent or mitigate the effects of these disorders.

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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 NameMetabolic Disorders Wide Range 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 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.

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