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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 Cystic Fibrosis Delta F508 Gene Mutation Test is 14 days.

What are the prerequisites for the test Cystic Fibrosis Delta F508 Gene Mutation Test

  • Patients must be referred by a healthcare provider
  • Patients must provide a blood or saliva sample for testing
  • Patients must not have taken antibiotics within the past two weeks before the test
  • Patients must not have had a lung transplant

What are the measure values for the test Cystic Fibrosis Delta F508 Gene Mutation Test

  • Positive/Negative
  • Positive: Presence of the Delta F508 mutation in the CFTR gene
  • Negative: Absence of the Delta F508 mutation in the CFTR gene

What does this test Cystic Fibrosis Delta F508 Gene Mutation Test identify?

Cystic Fibrosis Delta F508 Gene Mutation Test

The Cystic Fibrosis Delta F508 Gene Mutation Test identifies the presence of a specific mutation in the CFTR gene, known as Delta F508. This mutation is the most common cause of cystic fibrosis, a genetic disorder that affects the lungs and digestive system.

The test works by analyzing a sample of DNA, usually obtained through a blood or saliva sample. If the Delta F508 mutation is found, it indicates that the individual has a higher risk of developing cystic fibrosis or may already have the condition. Knowing whether a person carries this mutation can help in diagnosing and managing the disease.

Why is this test Cystic Fibrosis Delta F508 Gene Mutation Test taken?

The Cystic Fibrosis Delta F508 Gene Mutation Test is taken to detect mutations in the CFTR gene, specifically the Delta F508 mutation. This mutation is the most common cause of cystic fibrosis, a genetic disorder that affects the lungs, pancreas, liver, and intestines. By identifying this mutation, healthcare providers can diagnose cystic fibrosis earlier and provide appropriate treatment and management options for the patient. The test is usually recommended for individuals with a family history of cystic fibrosis or those experiencing symptoms of the condition.

Popular FAQs on Test

The Cystic Fibrosis Delta F508 Gene Mutation Test is a genetic test that looks for a specific mutation in the CFTR gene called Delta F508. This mutation is the most common cause of cystic fibrosis.
The test is performed to determine if a person carries the Delta F508 mutation in their CFTR gene. Carriers of this mutation have an increased risk of having a child with cystic fibrosis if their partner is also a carrier.
The test is usually done using a blood sample. The sample is sent to a laboratory where it is analyzed for the presence of the Delta F508 mutation.
No, the test is not painful. It involves a simple blood draw, which may cause slight discomfort but is generally well-tolerated.
A positive result means that the individual carries the Delta F508 mutation. They may have an increased risk of passing this mutation on to their children and should consider genetic counseling.

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