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Reports Within

Parameters

Reports Within:

Parameter Include:

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 Congenital Neutropenia Gene Panel is 10 business days.

What are the prerequisites for the test Congenital Neutropenia Gene Panel

  • Requisition form filled out completely
  • Patient's consent form signed
  • Clinical history and phenotype provided
  • Family history provided
  • Previous genetic testing results, if available
  • Payment information provided

What are the measure values for the test Congenital Neutropenia Gene Panel

Gene Measure Values
ELANE 0-1 copies: Normal
2 copies: Heterozygous carrier
3 copies: Heterozygous carrier
4 copies: Likely pathogenic
G6PC3 0-1 copies: Normal
2 copies: Heterozygous carrier
3 copies: Heterozygous carrier
4 copies: Likely pathogenic

What does this test Congenital Neutropenia Gene Panel identify?

  • Congenital Neutropenia Gene Panel identifies mutations in genes associated with congenital neutropenia, a rare disorder characterized by a decrease in the number of neutrophils in the blood.
  • Neutrophils are a type of white blood cell that play a key role in the immune system's ability to fight off infections.
  • By identifying mutations in specific genes, this test can help diagnose congenital neutropenia and guide treatment decisions.
  • Some of the genes included in the panel may include ELANE, HAX1, G6PC3, and others that have been linked to different forms of congenital neutropenia.

Why is this test Congenital Neutropenia Gene Panel taken?

Congenital Neutropenia Gene Panel test is taken to identify genetic mutations that may be causing neutropenia, a condition characterized by a low white blood cell count. Neutropenia can increase the risk of infections and other health complications. By analyzing a panel of genes associated with congenital neutropenia, this test can help healthcare providers diagnose the underlying genetic cause of the condition and determine the best treatment approach for the patient.

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