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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 Craniosynostosis Gene Panel is 21 days.

What are the prerequisites for the test Craniosynostosis Gene Panel

  • Medical provider order
  • Completed Test Requisition Form
  • Consent form signed by patient or legal guardian
  • Insurance information provided
  • Payment information provided (if self-pay)

What are the measure values for the test Craniosynostosis Gene Panel

Gene Measure Value
FGFR2 0.5
FGFR3 0.3
TWIST1 0.2

What does this test Craniosynostosis Gene Panel identify?

  • Craniosynostosis Gene Panel identifies mutations in genes associated with craniosynostosis, a condition where the bones in a baby's skull fuse together too early.
  • The panel includes analysis of genes such as FGFR1, FGFR2, FGFR3, and TWIST1, which are known to be involved in the development of craniosynostosis.
  • Identifying mutations in these genes can help in diagnosing craniosynostosis and determining the best treatment approach for affected individuals.
  • This test is particularly useful for individuals with a family history of craniosynostosis or those who have symptoms suggestive of the condition.

Why is this test Craniosynostosis Gene Panel taken?

Reason for taking Craniosynostosis Gene Panel Test

Craniosynostosis is a condition where one or more of the fibrous sutures in an infant's skull prematurely fuses, which can lead to abnormal skull growth and shape. This can sometimes be caused by genetic mutations.

The Craniosynostosis Gene Panel Test is taken to identify specific genetic mutations that may be responsible for causing craniosynostosis in an individual. By analyzing a panel of genes known to be associated with craniosynostosis, healthcare providers can determine the underlying genetic cause of the condition in a patient.

Knowing the genetic cause of craniosynostosis can help healthcare providers tailor treatment plans and provide more accurate prognosis for the patient. It can also help in genetic counseling for the patient and their family members.

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