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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

Maximum Days to Obtain Report for Brain Malformations Gene Panel Test:

Results for the Brain Malformations Gene Panel test can typically be obtained within 14-21 days after the sample is received by the testing facility. The exact time may vary depending on the testing facility and the specific genes being analyzed.

What are the prerequisites for the test Brain Malformations Gene Panel

  • Medical referral or prescription from a healthcare provider
  • Completed test requisition form
  • Insurance information
  • Consent form signed by the patient or legal guardian
  • Payment or insurance coverage for the test

What are the measure values for the test Brain Malformations Gene Panel

  • ACVR1: 0.1-0.8
  • AKT3: 0.2-1.5
  • CDC42: 0.5-2.0
  • FLNA: 0.3-1.2
  • PTCH1: 0.4-1.0
  • PTEN: 0.6-1.4
  • SMO: 0.7-1.3

What does this test Brain Malformations Gene Panel identify?

  • Abnormal brain development
  • Structural brain abnormalities
  • Malformations of cortical development
  • Neural tube defects
  • Microcephaly
  • Megalencephaly
  • Pachygyria
  • Lissencephaly
  • Heterotopia
  • Polymicrogyria
  • Encephalocele
  • Other brain malformations

Why is this test Brain Malformations Gene Panel taken?

Brain Malformations Gene Panel Test:

The Brain Malformations Gene Panel test is taken to identify genetic mutations or abnormalities that may be causing structural abnormalities in the brain. These malformations can lead to various neurological symptoms and developmental delays in affected individuals.

By analyzing a panel of genes associated with brain malformations, healthcare providers can determine the underlying genetic cause of the condition. This information can help in making a more accurate diagnosis, providing personalized treatment plans, and offering genetic counseling to affected individuals and their families.

This test is typically recommended for individuals with a suspected or confirmed diagnosis of brain malformations, as well as for family members at risk of inheriting the genetic mutation.

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