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Reports Within:

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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

Maximum Days for Limb Hypoplasia Reduction Defects Gene Panel Report

The report for the Limb Hypoplasia Reduction Defects Gene Panel test can be obtained within 10-14 business days from the date of sample collection.

What are the prerequisites for the test Limb Hypoplasia Reduction Defects Gene Panel

  • Sample type: Blood or saliva
  • Specimen requirements: 2-5 mL blood in EDTA tube or 2 mL saliva
  • Shipping conditions: Room temperature
  • Turnaround time: 3-4 weeks
  • Insurance coverage: Check with insurance provider

What are the measure values for the test Limb Hypoplasia Reduction Defects Gene Panel

Genes Tested Measure Value
SHH Reported as positive or negative
GLI3 Reported as positive or negative
HOXD13 Reported as positive or negative
TP63 Reported as positive or negative

What does this test Limb Hypoplasia Reduction Defects Gene Panel identify?

  • Limb Hypoplasia: This test identifies genetic mutations associated with limb hypoplasia, which refers to underdevelopment or incomplete development of limbs.
  • Reduction Defects: The panel can detect mutations that may cause reduction defects, which are abnormalities in the structure of limbs resulting in missing or malformed parts.

Why is this test Limb Hypoplasia Reduction Defects Gene Panel taken?

Reason for Limb Hypoplasia Reduction Defects Gene Panel Test

Reason for Test:

The Limb Hypoplasia Reduction Defects Gene Panel Test is taken to identify genetic mutations or abnormalities that may be causing limb hypoplasia or reduction defects in an individual. Limb hypoplasia refers to underdevelopment or incomplete formation of limbs, while reduction defects involve missing or underdeveloped parts of the limbs.

By analyzing specific genes associated with limb development, this test can help healthcare providers diagnose the underlying genetic cause of these abnormalities. This information is crucial for determining appropriate treatment strategies, providing genetic counseling, and guiding future reproductive decisions.

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