Your Cart Item
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

60
Mins

Homes

1M
Happy

Customers

4.9
Google

Rating

Certified

Labs

What is the maximum days the report can be obtained for the test

Maximum Report Turnaround Time for Nephrotic Syndrome Gene Panel Test

The report for the Nephrotic Syndrome Gene Panel test can be obtained within 14-21 business days from the date of sample collection.

What are the prerequisites for the test Nephrotic Syndrome Gene Panel

  • Clinical diagnosis of nephrotic syndrome
  • Family history of nephrotic syndrome
  • Referral by a healthcare provider
  • Consent for genetic testing

What are the measure values for the test Nephrotic Syndrome Gene Panel

Gene Measure Value
NPHS1 <= 0.02
NPHS2 <= 0.02
WT1 <= 0.02
LAMB2 <= 0.02
PLCE1 <= 0.02

What does this test Nephrotic Syndrome Gene Panel identify?

  • The Nephrotic Syndrome Gene Panel is a genetic test that identifies mutations in genes associated with nephrotic syndrome.
  • Nephrotic syndrome is a kidney disorder characterized by high levels of protein in the urine, low levels of protein in the blood, high cholesterol levels, and swelling (edema).
  • This panel specifically looks for mutations in genes such as NPHS1, NPHS2, WT1, TRPC6, and others that are known to be linked to the development of nephrotic syndrome.
  • Identifying these mutations can help healthcare providers make a more accurate diagnosis, determine the best course of treatment, and provide genetic counseling to affected individuals and their families.

Why is this test Nephrotic Syndrome Gene Panel taken?

Reason for Nephrotic Syndrome Gene Panel Test

Reason for Nephrotic Syndrome Gene Panel Test

Nephrotic Syndrome is a kidney disorder that causes your body to excrete too much protein in your urine. It can lead to complications such as blood clots, infections, and high cholesterol. The Nephrotic Syndrome Gene Panel Test is taken to identify genetic mutations that may be causing the syndrome.

This test is usually recommended when a person has symptoms of Nephrotic Syndrome, such as swelling, foamy urine, and fatigue. It can help determine the underlying cause of the syndrome and guide treatment decisions. The test can also be used to assess the risk of developing the syndrome in family members of affected individuals.

By analyzing specific genes associated with Nephrotic Syndrome, healthcare providers can provide personalized treatment plans and genetic counseling to manage the condition effectively. The results of the test can help in predicting disease progression and monitoring response to therapy.

No FAQs available.

Customer Google Rating