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Reports Within

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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 Zellweger Syndrome Gene Panel is 14 days.

What are the prerequisites for the test Zellweger Syndrome Gene Panel

  • Medical provider order
  • Consent form signed by the patient or legal guardian
  • Insurance pre-authorization, if required
  • Payment for the test, if not covered by insurance

What are the measure values for the test Zellweger Syndrome Gene Panel

  • PEX1 Gene: 0-2 copies
  • PEX2 Gene: 0-2 copies
  • PEX3 Gene: 0-2 copies
  • PEX5 Gene: 0-2 copies
  • PEX6 Gene: 0-2 copies
  • PEX10 Gene: 0-2 copies
  • PEX12 Gene: 0-2 copies
  • PEX13 Gene: 0-2 copies
  • PEX14 Gene: 0-2 copies

What does this test Zellweger Syndrome Gene Panel identify?

  • Zellweger Syndrome Gene Panel identifies mutations in genes associated with Zellweger syndrome, a rare genetic disorder that affects the functioning of peroxisomes in cells.
  • The panel tests for mutations in genes such as PEX1, PEX2, PEX3, PEX5, PEX6, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, and PEX26, which are involved in peroxisome biogenesis and function.
  • Identifying mutations in these genes can help diagnose Zellweger syndrome and guide treatment and management strategies for affected individuals.

Why is this test Zellweger Syndrome Gene Panel taken?

This test, Zellweger Syndrome Gene Panel, is taken to identify mutations in specific genes associated with Zellweger syndrome. Zellweger syndrome is a rare genetic disorder that affects the development of many parts of the body. It is caused by mutations in genes that are involved in the formation of peroxisomes, which are cell structures that help break down fatty acids and produce energy.

By analyzing the genes included in the panel, healthcare providers can determine if a person has mutations that are known to cause Zellweger syndrome. This information can help in making a diagnosis, providing appropriate medical care, and offering genetic counseling to affected individuals and their families.

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