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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 for obtaining a report for the Renal Tubular Acidosis Gene Panel test is 14 days.

What are the prerequisites for the test Renal Tubular Acidosis Gene Panel

  • Patients must be referred by a qualified healthcare provider
  • Patients must have symptoms or a family history suggestive of renal tubular acidosis
  • Patients should not be on any medications that may interfere with the test results
  • Patients should not have any severe kidney disease or other conditions that may impact the interpretation of the test

What are the measure values for the test Renal Tubular Acidosis Gene Panel

  • Carbonic anhydrase II (CA2) gene sequence analysis - Reported as detected or not detected
  • V-ATPase B1 (ATP6V1B1) gene sequence analysis - Reported as detected or not detected
  • V-ATPase B2 (ATP6V0A4) gene sequence analysis - Reported as detected or not detected
  • SLC4A1 gene sequence analysis - Reported as detected or not detected

What does this test Renal Tubular Acidosis Gene Panel identify?

  • Renal Tubular Acidosis Gene Panel identifies mutations in genes associated with renal tubular acidosis.
  • It specifically looks for abnormalities in genes such as ATP6V1B1, ATP6V0A4, SLC4A1, and CA2 that can lead to the development of renal tubular acidosis.
  • Renal tubular acidosis is a condition characterized by the inability of the kidneys to effectively remove acid from the blood, leading to a buildup of acid in the body.
  • Identifying mutations in these genes can help diagnose renal tubular acidosis and guide treatment decisions.

Why is this test Renal Tubular Acidosis Gene Panel taken?

The Renal Tubular Acidosis Gene Panel test is taken to diagnose and assess a group of genetic disorders that affect the kidneys' ability to regulate acid-base balance in the body. These disorders can lead to a buildup of acid in the blood and urine, which can result in symptoms such as weakness, fatigue, muscle cramps, and abnormal heart rhythms.

This test is typically ordered when a healthcare provider suspects that a patient may have a genetic form of renal tubular acidosis based on their symptoms, medical history, and family history. The test can help identify specific genetic mutations that are causing the disorder, which can help guide treatment decisions and provide valuable information for genetic counseling.

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