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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

The maximum days the report can be obtained for the test Medullary Cystic Kidney Disease Gene Panel is 21 days.

What are the prerequisites for the test Medullary Cystic Kidney Disease Gene Panel

  • Patients suspected of having Medullary Cystic Kidney Disease
  • Family history of Medullary Cystic Kidney Disease
  • Referral from a healthcare provider
  • Consent form signed by the patient or legal guardian

What are the measure values for the test Medullary Cystic Kidney Disease Gene Panel

  • Gene Panel: Medullary Cystic Kidney Disease
  • Measures:
    • Genes Tested: PKHD1, HNF1B, UMOD, REN
    • Variant Types Detected: Deletion/Duplication, Nucleotide Change
    • Methodology: Next Generation Sequencing (NGS)
    • Turnaround Time: 4-6 weeks

What does this test Medullary Cystic Kidney Disease Gene Panel identify?

Medullary Cystic Kidney Disease Gene Panel

The Medullary Cystic Kidney Disease Gene Panel is a test that identifies mutations in genes associated with medullary cystic kidney disease (MCKD). MCKD is a rare genetic disorder that causes progressive kidney dysfunction and can lead to end-stage renal disease.

  • Genes Tested: The panel typically includes testing for mutations in genes such as MUC1, UMOD, REN, and HNF1B.
  • Identification of Mutations: By analyzing the DNA of an individual, this test can identify specific genetic mutations that are linked to MCKD.
  • Clinical Utility: The results of this test can help in confirming a diagnosis of MCKD, predicting disease progression, and guiding treatment options.

Why is this test Medullary Cystic Kidney Disease Gene Panel taken?

Medullary Cystic Kidney Disease Gene Panel test is taken to diagnose Medullary Cystic Kidney Disease (MCKD), a rare genetic disorder that affects the kidneys. This test looks for mutations in specific genes that are known to be associated with MCKD. By identifying these mutations, doctors can confirm a diagnosis of MCKD and provide appropriate treatment and management for the condition.

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