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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 test Polycystic Liver Disease Gene Panel is 14 days.

What are the prerequisites for the test Polycystic Liver Disease Gene Panel

  • Sample Type: Whole blood
  • Sample Container: Lavender top (EDTA) tube
  • Sample Volume: 3-5 mL
  • Storage and Transport: Ship at room temperature
  • Turnaround Time: 15-21 days

What are the measure values for the test Polycystic Liver Disease Gene Panel

  • Gene Panel: Polycystic Liver Disease
  • Measures:
    • PRKCSH gene variant detection
    • SEC63 gene variant detection
    • LRP5 gene variant detection
    • TSC2 gene variant detection
    • PKD1 gene variant detection
    • PKD2 gene variant detection

What does this test Polycystic Liver Disease Gene Panel identify?

  • Polycystic Liver Disease Gene Panel identifies mutations in genes associated with polycystic liver disease.
  • These genes include PRKCSH, SEC63, LRP5, ALG8, ALG9, ALG12, ALG2, ALG3, ALG6, ALG9, ALG10, ALG11, and CARS1.
  • These mutations can cause abnormal growth of cysts in the liver, leading to symptoms such as abdominal pain, bloating, and liver enlargement.
  • Identifying these mutations can help in the diagnosis and management of polycystic liver disease.

Why is this test Polycystic Liver Disease Gene Panel taken?

Polycystic Liver Disease Gene Panel test is taken to diagnose and confirm the presence of polycystic liver disease (PCLD). PCLD is a genetic disorder characterized by the development of multiple cysts in the liver, which can lead to symptoms such as abdominal pain, bloating, and complications such as bile duct obstructions.

The gene panel test analyzes specific genes known to be associated with PCLD, such as PRKCSH, SEC63, and LRP5. By identifying mutations in these genes, healthcare providers can make an accurate diagnosis of PCLD and provide appropriate treatment and management options for patients.

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