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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 report for the test Disorders Of Fatty Acid & Peroxisomal Test can be obtained within a maximum of 7 days.

What are the prerequisites for the test Disorders Of Fatty Acid & Peroxisomal Test

  • Medical history evaluation
  • Physical examination
  • Family history assessment
  • Laboratory tests such as blood tests, urine tests, and genetic testing
  • Consultation with a genetic counselor or specialist

What are the measure values for the test Disorders Of Fatty Acid & Peroxisomal Test

  • Plasma very long chain fatty acids (VLCFAs): Normal range: 0.2-0.7 μmol/L
  • Phytanic acid: Normal range: <0.1 μmol/L
  • Pristanic acid: Normal range: <0.1 μmol/L
  • Plasma acylcarnitines C16, C18: Normal range: <0.2 μmol/L

What does this test Disorders Of Fatty Acid & Peroxisomal Test identify?

This test identifies disorders related to fatty acid metabolism and peroxisomal function. These disorders can affect the body's ability to break down and utilize fatty acids for energy, leading to a buildup of toxic byproducts and potentially serious health complications.

Some of the specific disorders that can be identified through this test include:

  • Medium-chain acyl-CoA dehydrogenase deficiency
  • Long-chain hydroxyacyl-CoA dehydrogenase deficiency
  • Very long-chain acyl-CoA dehydrogenase deficiency
  • X-linked adrenoleukodystrophy
  • Zellweger syndrome

Why is this test Disorders Of Fatty Acid & Peroxisomal Test taken?

Disorders Of Fatty Acid & Peroxisomal Test

Why is this test taken?

This test is performed to diagnose and monitor disorders related to fatty acid metabolism and peroxisomal function. These disorders can affect the body's ability to break down and utilize fatty acids for energy, leading to a variety of symptoms and complications.

Some of the conditions that may be detected through this test include:

  • Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency
  • Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency
  • Peroxisomal disorders such as Zellweger syndrome
  • Beta-oxidation disorders

By measuring the levels of various fatty acids and other metabolites in the blood, urine, or other tissues, healthcare providers can identify these disorders early on and provide appropriate treatment and management strategies.

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