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Parameters

Reports Within:

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Requisites
Measures

Number of red blood cells in the blood

Identifies

Red blood cell disorders

Measures: Number of red blood cells in the blood

Identifies: Red blood cell disorders

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What is the maximum days the report can be obtained for the test

The maximum days the report can be obtained for the test Disorders Of Purines, Pyrimidines & Nucleotide Metabolism Test is typically 7-10 business days. However, this time frame may vary depending on the specific laboratory or healthcare provider performing the test.

What are the prerequisites for the test Disorders Of Purines, Pyrimidines & Nucleotide Metabolism Test

  • Understanding of basic biochemistry concepts
  • Knowledge of purine, pyrimidine, and nucleotide metabolism pathways
  • Familiarity with the enzymes involved in purine and pyrimidine metabolism
  • Ability to interpret laboratory results related to purine and pyrimidine disorders

What are the measure values for the test Disorders Of Purines, Pyrimidines & Nucleotide Metabolism Test

  • Uric Acid: 2.4-6.0 mg/dL
  • Hypoxanthine: 0-2.3 mg/dL
  • Xanthine: 0-2.0 mg/dL
  • Adenine: 0-0.5 mg/dL
  • Guanylate: 0-0.5 mg/dL

What does this test Disorders Of Purines, Pyrimidines & Nucleotide Metabolism Test identify?

Disorders Of Purines, Pyrimidines & Nucleotide Metabolism Test

This test is used to identify various disorders related to purines, pyrimidines, and nucleotide metabolism. These disorders include:

  • Lesch-Nyhan syndrome
  • Gout
  • Adenosine deaminase deficiency
  • Hypoxanthine-guanine phosphoribosyltransferase deficiency
  • Orotic aciduria

Why is this test Disorders Of Purines, Pyrimidines & Nucleotide Metabolism Test taken?

Disorders of purines, pyrimidines, and nucleotide metabolism test is taken to diagnose and monitor various genetic conditions that affect the metabolism of these important molecules in the body. These disorders can lead to a range of symptoms and complications, including intellectual disability, developmental delay, seizures, muscle weakness, and kidney problems.

This test is usually recommended when a healthcare provider suspects that a patient may have a genetic disorder that affects purine, pyrimidine, or nucleotide metabolism based on their symptoms, medical history, or family history. The test can help confirm a diagnosis, guide treatment decisions, and provide information about the risk of passing the condition on to future children.

In some cases, this test may also be used to monitor the effectiveness of treatment for a known disorder of purine, pyrimidine, or nucleotide metabolism, or to assess the risk of complications associated with the condition.

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