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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

Microcephaly Gene Panel Test

The maximum days to obtain the report for the Microcephaly Gene Panel test is 14 days.

What are the prerequisites for the test Microcephaly Gene Panel

  • Patients suspected of having microcephaly based on clinical presentation
  • Patients with a family history of microcephaly
  • Patients with developmental delay or intellectual disability
  • Patients with seizures
  • Patients with abnormal brain imaging findings suggestive of microcephaly

What are the measure values for the test Microcephaly Gene Panel

  • Gene: ASPM
  • Measure Value: 0-1 pathogenic variant(s) detected
  • Interpretation: Negative
  • Gene: CDK5RAP2
  • Measure Value: 0-1 pathogenic variant(s) detected
  • Interpretation: Negative
  • Gene: MCPH1
  • Measure Value: 0-1 pathogenic variant(s) detected
  • Interpretation: Negative

What does this test Microcephaly Gene Panel identify?

Microcephaly Gene Panel Identification:

The Microcephaly Gene Panel is a genetic test that aims to identify mutations or variations in genes associated with microcephaly. Microcephaly is a condition characterized by a smaller than average head size and is often linked to intellectual disabilities and developmental delays.

This panel specifically targets genes known to be involved in the development and growth of the brain, particularly during prenatal and early postnatal stages. By analyzing these genes, the test can help identify potential genetic causes of microcephaly in individuals.

The test results can provide valuable insights for healthcare providers in diagnosing and managing microcephaly in patients, as well as offering genetic counseling and family planning options for affected individuals and their families.

Why is this test Microcephaly Gene Panel taken?

Microcephaly Gene Panel Test is taken to diagnose individuals with microcephaly, a condition characterized by a smaller than average head size due to abnormal brain development. This test helps in identifying genetic mutations that may be responsible for causing microcephaly. By analyzing a panel of genes associated with microcephaly, healthcare providers can determine the specific genetic cause of the condition in a patient, which can help in making appropriate treatment and management decisions.

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