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CYSTIC FIBROSIS DNA TEST REQUISITION For testing at the Molecular Diagnostics Laboratory of The Nebraska Medical Center This form should accompany specimen or can be faxed directly to the laboratory
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How to fill out cystic fibrosis dna test

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How to fill out cystic fibrosis dna test

01
Step 1: Collect a DNA sample from the individual to be tested for cystic fibrosis.
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Step 2: Ensure the sample is properly preserved to prevent DNA degradation. This can be done by storing the sample in a sterile container or using a DNA preservation kit.
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Step 3: Prepare the DNA sample for testing by extracting the DNA from the cells. This can be done using various methods such as a DNA extraction kit or a laboratory-based extraction procedure.
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Step 4: Amplify the extracted DNA to obtain a sufficient amount for testing. This can be achieved through a process called Polymerase Chain Reaction (PCR).
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Step 5: Perform the cystic fibrosis DNA test using a specific testing method such as Sanger sequencing or a DNA microarray.
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Step 6: Analyze the test results to determine if the individual carries any mutations or variations associated with cystic fibrosis.
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Step 7: Interpret the results by comparing them to known references or databases of cystic fibrosis mutations.
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Step 8: Provide a comprehensive report of the test results, including the presence or absence of cystic fibrosis-associated mutations.
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Step 9: Discuss the test results with a healthcare provider or genetic counselor to understand the implications and potential treatment options.

Who needs cystic fibrosis dna test?

01
Individuals who have a family history of cystic fibrosis.
02
Couples who are planning to have a child and want to assess their risk of having a child with cystic fibrosis.
03
Individuals with symptoms or suspected diagnosis of cystic fibrosis.
04
Parents of newborns who have tested positive for cystic fibrosis through newborn screening.
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Cystic fibrosis DNA test is a genetic test that detects mutations in the CFTR gene, which can cause cystic fibrosis.
Individuals who suspect they may carry a CFTR gene mutation or have a family history of cystic fibrosis may choose to undergo cystic fibrosis DNA testing.
Cystic fibrosis DNA testing is typically done through a genetic testing kit provided by a healthcare provider. The individual will provide a DNA sample, usually through a cheek swab or blood sample, and send it to a laboratory for analysis.
The purpose of cystic fibrosis DNA testing is to identify any mutations in the CFTR gene that could lead to the development of cystic fibrosis in an individual or their offspring.
The cystic fibrosis DNA test will report any mutations found in the CFTR gene that are associated with cystic fibrosis. It may also include information on the individual's carrier status and risk of passing on the mutation to their children.
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