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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

Maximum Days for Cystic Fibrosis Mutation Screening Test Report

Maximum Days for Cystic Fibrosis Mutation Screening Test Report

The maximum days to obtain the report for the Cystic Fibrosis Mutation Screening Test is typically 7-10 days. However, this may vary depending on the laboratory and specific circumstances.

What are the prerequisites for the test Cystic Fibrosis Mutation Screening Test

  • There are no specific prerequisites for the Cystic Fibrosis Mutation Screening Test.
  • However, it is recommended that individuals with a family history of cystic fibrosis or those who are carriers of the gene mutation undergo this test.
  • Prior to the test, individuals may be asked to provide a blood sample or a buccal swab for genetic testing.

What are the measure values for the test Cystic Fibrosis Mutation Screening Test

  • Delta F508 Mutation: Detected or Not Detected
  • W1282X Mutation: Detected or Not Detected
  • G542X Mutation: Detected or Not Detected
  • N1303K Mutation: Detected or Not Detected
  • 3120+1G>A Mutation: Detected or Not Detected

What does this test Cystic Fibrosis Mutation Screening Test identify?

  • Cystic Fibrosis Mutation Screening Test
  • Identifies mutations in the CFTR gene that are associated with Cystic Fibrosis
  • Helps in diagnosing Cystic Fibrosis in individuals who may be carriers or affected by the disease
  • Can provide information on the risk of passing on the mutated gene to offspring

Why is this test Cystic Fibrosis Mutation Screening Test taken?

The Cystic Fibrosis Mutation Screening Test is taken to identify mutations in the CFTR gene that can cause cystic fibrosis. Cystic fibrosis is a genetic disorder that affects the lungs and digestive system, leading to difficulties in breathing and digesting food. By identifying mutations in the CFTR gene, healthcare providers can diagnose cystic fibrosis and provide appropriate treatment and management options for individuals with the condition.

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