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

The maximum days the report can be obtained for the test Congenital Adrenal Hyperplasia (CAH) Gene Analysis Test is 14 days.

What are the prerequisites for the test Congenital Adrenal Hyperplasia (CAH) Gene Analysis Test

  • Collection Container: Lavender (EDTA) or Yellow (ACD) top tube
  • Methodology: Polymerase Chain Reaction (PCR) and DNA sequencing
  • Turnaround Time: 7-10 days
  • Specimen Requirements: 3-5 mL whole blood
  • Storage/Transport Temperature: Room temperature
  • Rejection Criteria: Improper labeling, clotted specimen, quantity not sufficient

What are the measure values for the test Congenital Adrenal Hyperplasia (CAH) Gene Analysis Test

  1. 17-alpha-Hydroxyprogesterone (17-OHP) level in blood
  2. Genetic analysis for mutations in the CYP21A2 gene
  3. ACTH stimulation test
  4. 24-hour urine steroid profile

What does this test Congenital Adrenal Hyperplasia (CAH) Gene Analysis Test identify?

  • Identifies mutations in the genes that are associated with Congenital Adrenal Hyperplasia (CAH)
  • Determines the specific type of CAH a person may have
  • Helps in diagnosing CAH in newborns and infants
  • Assists in genetic counseling for families with a history of CAH

Why is this test Congenital Adrenal Hyperplasia (CAH) Gene Analysis Test taken?

The Congenital Adrenal Hyperplasia (CAH) Gene Analysis Test is taken to diagnose a genetic disorder that affects the adrenal glands. CAH is a group of inherited disorders that affect the body's ability to produce hormones that regulate essential functions such as metabolism, immune response, and stress. This test is specifically done to identify mutations in the genes responsible for CAH, which can help guide treatment and management of the condition.

No FAQs available.

Customer Google Rating