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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 for obtaining the report for the Polydactyly Syndactyly Triphalangism Gene Panel test is 14 days.

What are the prerequisites for the test Polydactyly Syndactyly Triphalangism Gene Panel

  • Patient must have a suspected or confirmed diagnosis of polydactyly, syndactyly, or triphalangism
  • Physician's order
  • Complete the test requisition form
  • Provide a blood or saliva sample
  • Consent form signed by the patient or legal guardian

What are the measure values for the test Polydactyly Syndactyly Triphalangism Gene Panel

  • Polydactyly: Presence or absence of extra fingers or toes
  • Syndactyly: Presence or absence of webbing between fingers or toes
  • Triphalangism: Presence or absence of an extra phalanx in fingers or toes

What does this test Polydactyly Syndactyly Triphalangism Gene Panel identify?

  • Polydactyly: This test identifies genetic variants associated with polydactyly, a condition characterized by extra fingers or toes.
  • Syndactyly: The panel looks for genetic mutations linked to syndactyly, a condition where fingers or toes are fused together.
  • Triphalangism: This test also detects genetic changes related to triphalangism, a rare condition where an extra bone is present in the fingers or toes.

Why is this test Polydactyly Syndactyly Triphalangism Gene Panel taken?

The Polydactyly Syndactyly Triphalangism Gene Panel test is taken to identify genetic mutations associated with conditions such as polydactyly, syndactyly, and triphalangism. These conditions involve abnormalities in the development of fingers and toes, leading to extra digits, fused digits, or additional phalanges.

By analyzing specific genes known to be involved in these conditions, the test can help diagnose individuals with these abnormalities and provide information for genetic counseling, management, and treatment options.

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