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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 Peroxisomal Disorders Gene Panel (Includes Adrenoleukodystrophy) is typically 14-21 days from the date of sample receipt at the testing facility.

What are the prerequisites for the test Peroxisomal Disorders Gene Panel (Includes Adrenoleukodystrophy)

  • Specimen Type: Whole blood
  • Specimen Volume: 3-5 mL
  • Collection Container/Tube: Lavender top (EDTA)
  • Storage Instructions: Maintain specimen at room temperature or refrigerate at 4°C
  • Stability: Ambient: 72 hours; Refrigerated: 2 weeks
  • Rejection Criteria: Hemolysis

What are the measure values for the test Peroxisomal Disorders Gene Panel (Includes Adrenoleukodystrophy)

  • ACOX1 Gene Sequencing
  • ABCD1 Gene Sequencing
  • AGPS Gene Sequencing
  • PEX1 Gene Sequencing
  • PEX2 Gene Sequencing
  • PEX5 Gene Sequencing
  • PEX6 Gene Sequencing
  • PEX10 Gene Sequencing
  • PEX11B Gene Sequencing
  • PEX12 Gene Sequencing
  • PEX13 Gene Sequencing
  • PEX14 Gene Sequencing
  • PEX16 Gene Sequencing
  • PEX19 Gene Sequencing
  • PEX26 Gene Sequencing

What does this test Peroxisomal Disorders Gene Panel (Includes Adrenoleukodystrophy) identify?

  • This test identifies mutations in genes associated with peroxisomal disorders, including adrenoleukodystrophy.
  • Peroxisomal disorders are a group of genetic disorders that affect the function of peroxisomes, cellular organelles involved in various metabolic processes.
  • Adrenoleukodystrophy is a specific peroxisomal disorder that primarily affects the nervous system and adrenal glands.
  • The gene panel test analyzes specific genes known to be associated with peroxisomal disorders, helping to diagnose individuals with these conditions.
  • Identifying mutations in these genes can provide valuable information for genetic counseling, treatment planning, and disease management.

Why is this test Peroxisomal Disorders Gene Panel (Includes Adrenoleukodystrophy) taken?

This test is taken to detect Peroxisomal Disorders, which are a group of rare genetic disorders that affect the function of peroxisomes in the cells. Peroxisomes are small organelles in the cell that are responsible for various important functions, including breaking down fatty acids and detoxifying harmful substances.

The Peroxisomal Disorders Gene Panel (Includes Adrenoleukodystrophy) specifically looks for mutations in genes associated with peroxisomal disorders, including Adrenoleukodystrophy (ALD), a severe form of peroxisomal disorder that affects the nervous system.

By identifying mutations in these genes, healthcare providers can diagnose peroxisomal disorders early, allowing for appropriate treatment and management to be initiated. Early detection and intervention can help improve outcomes and quality of life for individuals with peroxisomal disorders.

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